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dbVar

Database of genomic structural variation

nsv3171178

Organism: Homo sapiens

Study:nstd152 (Chaisson et al. 2019)
Variant Type:complex substitution
Method Type:Optical mapping, Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:18,693

Publication(s):Chaisson et al. 2019

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: 1003 SVs from 84 studies. See in: genome view

Submitted genomic195,769,990-195,788,682

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3171178	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	195,769,990	195,788,682
nsv3171178	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	195,496,861	195,515,553

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14410352	complex substitution	SAMN00001696	Optical mapping, Sequencing	Optical mapping, Sequence alignment, de novo and local sequence assembly	45,591

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14410352	Submitted genomic		GRCh38 (hg38)		NC_000003.12	Chr3	195,769,990	195,788,682
nssv14410352	Remapped	Perfect	GRCh37.p13	First Pass	NC_000003.11	Chr3	195,496,861	195,515,553

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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