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dbVar

Database of genomic structural variation

nsv6106219

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: 220 SVs from 19 studies. See in: genome view

Submitted genomic54,172,066-54,172,066

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6106219	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	54,172,066	54,172,066
nsv6106219	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	51,698,436	51,698,436

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17632932	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17632932	Submitted genomic		NC_000018.10:g.541 72066_54172067ins3 09	GRCh38 (hg38)		NC_000018.10	Chr18	54,172,066	54,172,066
nssv17632932	Remapped	Perfect	NC_000018.9:g.5169 8436_51698437ins30 9	GRCh37.p13	First Pass	NC_000018.9	Chr18	51,698,436	51,698,436

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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