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dbVar

Database of genomic structural variation

nsv6057654

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: 142 SVs from 37 studies. See in: genome view

Submitted genomic113,603,790-113,603,790

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6057654	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	113,603,790	113,603,790
nsv6057654	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	114,361,367	114,361,367

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17529177	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17529177	Submitted genomic		NC_000002.12:g.113 603790_113603791in s173	GRCh38 (hg38)		NC_000002.12	Chr2	113,603,790	113,603,790
nssv17529177	Remapped	Perfect	NC_000002.11:g.114 361367_114361368in s173	GRCh37.p13	First Pass	NC_000002.11	Chr2	114,361,367	114,361,367

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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