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dbVar

Database of genomic structural variation

nsv5619443

Organism: Homo sapiens

Study:nstd207 (Ebert 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):Ebert 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: 155 SVs from 32 studies. See in: genome view

Submitted genomic149,545,740-149,545,740

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5619443	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	149,545,740	149,545,740
nsv5619443	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003871055.3	Chr1\|NW_00 3871055.3	6,361,153	6,361,153

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060606	insertion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17060606	Submitted genomic		NC_000001.11:g.149 545740_149545741in s491	GRCh38 (hg38)		NC_000001.11	Chr1	149,545,740	149,545,740
nssv17060606	Remapped	Perfect	NW_003871055.3:g.6 361153_6361154ins4 91	GRCh37.p13	First Pass	NW_003871055.3	Chr1\|NW_00 3871055.3	6,361,153	6,361,153

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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