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dbVar

Database of genomic structural variation

nsv5614793

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: 153 SVs from 35 studies. See in: genome view

Submitted genomic68,242,306-68,242,306

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5614793	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	68,242,306	68,242,306
nsv5614793	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	69,108,024	69,108,024

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17135800	insertion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17135800	Submitted genomic		NC_000004.12:g.682 42306_68242307ins1 20	GRCh38 (hg38)		NC_000004.12	Chr4	68,242,306	68,242,306
nssv17135800	Remapped	Perfect	NC_000004.11:g.691 08024_69108025ins1 20	GRCh37.p13	First Pass	NC_000004.11	Chr4	69,108,024	69,108,024

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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