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dbVar

Database of genomic structural variation

nsv6098051

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: 88 SVs from 23 studies. See in: genome view

Submitted genomic47,797,234-47,797,234

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6098051	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	47,797,234	47,797,234
nsv6098051	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	48,191,017	48,191,017

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17604478	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17604478	Submitted genomic		NC_000012.12:g.477 97234_47797235ins2 98	GRCh38 (hg38)		NC_000012.12	Chr12	47,797,234	47,797,234
nssv17604478	Remapped	Perfect	NC_000012.11:g.481 91017_48191018ins2 98	GRCh37.p13	First Pass	NC_000012.11	Chr12	48,191,017	48,191,017

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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