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dbVar

Database of genomic structural variation

nsv6103346

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

Submitted genomic44,745,397-44,745,397

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6103346	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	44,745,397	44,745,397
nsv6103346	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	43,374,038	43,374,038

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17627822	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17627822	Submitted genomic		NC_000020.11:g.447 45397_44745398ins5 9	GRCh38 (hg38)		NC_000020.11	Chr20	44,745,397	44,745,397
nssv17627822	Remapped	Perfect	NC_000020.10:g.433 74038_43374039ins5 9	GRCh37.p13	First Pass	NC_000020.10	Chr20	43,374,038	43,374,038

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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