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dbVar

Database of genomic structural variation

nsv6051056

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Wu et al. 2021

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: 127 SVs from 26 studies. See in: genome view

Submitted genomic111,755,128-111,755,128

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6051056	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	111,755,128	111,755,128
nsv6051056	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	112,297,750	112,297,750

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17529829	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17529829	Submitted genomic		NC_000001.11:g.111 755128_111755129in s53	GRCh38 (hg38)		NC_000001.11	Chr1	111,755,128	111,755,128
nssv17529829	Remapped	Perfect	NC_000001.10:g.112 297750_112297751in s53	GRCh37.p13	First Pass	NC_000001.10	Chr1	112,297,750	112,297,750

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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