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dbVar

Database of genomic structural variation

nsv5611541

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: 566 SVs from 57 studies. See in: genome view

Submitted genomic147,653,119-147,653,119

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5611541	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	147,653,119	147,653,119
nsv5611541	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003871055.3	Chr1\|NW_00 3871055.3	4,468,532	4,468,532

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060549	insertion	NA24385	Sequencing	Sequence alignment	2,573

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17060549	Submitted genomic		NC_000001.11:g.147 653119_147653120in s307	GRCh38 (hg38)		NC_000001.11	Chr1	147,653,119	147,653,119
nssv17060549	Remapped	Perfect	NW_003871055.3:g.4 468532_4468533ins3 07	GRCh37.p13	First Pass	NW_003871055.3	Chr1\|NW_00 3871055.3	4,468,532	4,468,532

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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