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dbVar

Database of genomic structural variation

nsv6104949

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: 125 SVs from 25 studies. See in: genome view

Submitted genomic45,866,822-45,866,822

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6104949	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	45,866,822	45,866,822
nsv6104949	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	44,495,461	44,495,461

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17633027	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17633027	Submitted genomic		NC_000020.11:g.458 66822_45866823ins2 91	GRCh38 (hg38)		NC_000020.11	Chr20	45,866,822	45,866,822
nssv17633027	Remapped	Perfect	NC_000020.10:g.444 95461_44495462ins2 91	GRCh37.p13	First Pass	NC_000020.10	Chr20	44,495,461	44,495,461

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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