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dbVar

Database of genomic structural variation

nsv6048364

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: 113 SVs from 22 studies. See in: genome view

Submitted genomic92,223,940-92,223,940

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6048364	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	92,223,940	92,223,940
nsv6048364	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	92,689,497	92,689,497

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17522810	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17522810	Submitted genomic		NC_000001.11:g.922 23940_92223941ins3 20	GRCh38 (hg38)		NC_000001.11	Chr1	92,223,940	92,223,940
nssv17522810	Remapped	Perfect	NC_000001.10:g.926 89497_92689498ins3 20	GRCh37.p13	First Pass	NC_000001.10	Chr1	92,689,497	92,689,497

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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