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dbVar

Database of genomic structural variation

nsv5647049

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: 953 SVs from 56 studies. See in: genome view

Submitted genomic15,869,864-15,869,864

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5647049	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	15,869,864	15,869,864
nsv5647049	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	15,963,721	15,963,721

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17080310	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17080310	Submitted genomic		NC_000016.10:g.158 69864_15869865ins3 75	GRCh38 (hg38)		NC_000016.10	Chr16	15,869,864	15,869,864
nssv17080310	Remapped	Perfect	NC_000016.9:g.1596 3721_15963722ins37 5	GRCh37.p13	First Pass	NC_000016.9	Chr16	15,963,721	15,963,721

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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