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dbVar

Database of genomic structural variation

nsv7099286

Organism: Homo sapiens

Study:nstd231 (Ali et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:4
Validation:Not tested
Clinical Assertions: No
Region Size:48,221

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 367 SVs from 50 studies. See in: genome view

Remapped(Score: Perfect):99,646,185-99,694,405

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099286	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	99,646,185	99,694,405
nsv7099286	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	99,516,916	99,565,136

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18793005	deletion	SNP array	SNP genotyping analysis
nssv18793012	deletion	SNP array	SNP genotyping analysis
nssv18793030	deletion	SNP array	SNP genotyping analysis
nssv18793037	deletion	SNP array	SNP genotyping analysis

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18793005	Remapped	Perfect	NC_000011.10:g.(99 646185_?)_(?_99694 405)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,646,185	99,694,405
nssv18793012	Remapped	Perfect	NC_000011.10:g.(99 646185_?)_(?_99694 405)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,646,185	99,694,405
nssv18793030	Remapped	Perfect	NC_000011.10:g.(99 646185_?)_(?_99694 405)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,646,185	99,694,405
nssv18793037	Remapped	Perfect	NC_000011.10:g.(99 646185_?)_(?_99694 405)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,646,185	99,694,405
nssv18793005	Submitted genomic		NC_000011.9:g.(995 16916_?)_(?_995651 36)del	GRCh37 (hg19)		NC_000011.9	Chr11	99,516,916	99,565,136
nssv18793012	Submitted genomic		NC_000011.9:g.(995 16916_?)_(?_995651 36)del	GRCh37 (hg19)		NC_000011.9	Chr11	99,516,916	99,565,136
nssv18793030	Submitted genomic		NC_000011.9:g.(995 16916_?)_(?_995651 36)del	GRCh37 (hg19)		NC_000011.9	Chr11	99,516,916	99,565,136
nssv18793037	Submitted genomic		NC_000011.9:g.(995 16916_?)_(?_995651 36)del	GRCh37 (hg19)		NC_000011.9	Chr11	99,516,916	99,565,136

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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