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dbVar

Database of genomic structural variation

nsv6098342

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: 118 SVs from 20 studies. See in: genome view

Submitted genomic99,855,556-99,855,556

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6098342	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	99,855,556	99,855,556
nsv6098342	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	102,617,838	102,617,838

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17581001	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17581001	Submitted genomic		NC_000009.12:g.998 55556_99855557ins6 6	GRCh38 (hg38)		NC_000009.12	Chr9	99,855,556	99,855,556
nssv17581001	Remapped	Perfect	NC_000009.11:g.102 617838_102617839in s66	GRCh37.p13	First Pass	NC_000009.11	Chr9	102,617,838	102,617,838

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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