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dbVar

Database of genomic structural variation

nsv6112614

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: 562 SVs from 38 studies. See in: genome view

Submitted genomic79,944,915-79,944,915

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112614	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	79,944,915	79,944,915
nsv6112614	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	77,704,915	77,704,915

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17619419	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17619419	Submitted genomic		NC_000018.10:g.799 44915_79944916ins5 3	GRCh38 (hg38)		NC_000018.10	Chr18	79,944,915	79,944,915
nssv17619419	Remapped	Perfect	NC_000018.9:g.7770 4915_77704916ins53	GRCh37.p13	First Pass	NC_000018.9	Chr18	77,704,915	77,704,915

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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