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dbVar

Database of genomic structural variation

nsv6060773

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 25 studies. See in: genome view

Submitted genomic146,104,185-146,104,185

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6060773	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	146,104,185	146,104,185
nsv6060773	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	147,025,337	147,025,337

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17557110	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17557110	Submitted genomic		NC_000004.12:g.146 104185_146104186in s71	GRCh38 (hg38)		NC_000004.12	Chr4	146,104,185	146,104,185
nssv17557110	Remapped	Perfect	NC_000004.11:g.147 025337_147025338in s71	GRCh37.p13	First Pass	NC_000004.11	Chr4	147,025,337	147,025,337

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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