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dbVar

Database of genomic structural variation

nsv6084314

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: 105 SVs from 21 studies. See in: genome view

Submitted genomic57,403,381-57,403,381

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6084314	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	57,403,381	57,403,381
nsv6084314	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	57,437,293	57,437,293

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17633528	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17633528	Submitted genomic		NC_000016.10:g.574 03381_57403382ins1 38	GRCh38 (hg38)		NC_000016.10	Chr16	57,403,381	57,403,381
nssv17633528	Remapped	Perfect	NC_000016.9:g.5743 7293_57437294ins13 8	GRCh37.p13	First Pass	NC_000016.9	Chr16	57,437,293	57,437,293

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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