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dbVar

Database of genomic structural variation

nsv6067278

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: 119 SVs from 32 studies. See in: genome view

Submitted genomic99,363,847-99,363,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6067278	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	99,363,847	99,363,847
nsv6067278	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	98,961,470	98,961,470

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17562534	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17562534	Submitted genomic		NC_000007.14:g.993 63847_99363848ins3 08	GRCh38 (hg38)		NC_000007.14	Chr7	99,363,847	99,363,847
nssv17562534	Remapped	Perfect	NC_000007.13:g.989 61470_98961471ins3 08	GRCh37.p13	First Pass	NC_000007.13	Chr7	98,961,470	98,961,470

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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