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dbVar

Database of genomic structural variation

nsv5672213

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: 117 SVs from 38 studies. See in: genome view

Submitted genomic62,058,987-62,058,987

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672213	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	62,058,987	62,058,987
nsv5672213	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	60,634,043	60,634,043

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17117590	insertion	HG03683	Sequencing	Sequence alignment	2,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17117590	Submitted genomic		NC_000020.11:g.620 58987_62058988ins1 473	GRCh38 (hg38)		NC_000020.11	Chr20	62,058,987	62,058,987
nssv17117590	Remapped	Perfect	NC_000020.10:g.606 34043_60634044ins1 473	GRCh37.p13	First Pass	NC_000020.10	Chr20	60,634,043	60,634,043

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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