A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179102



Internal ID21317898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203966703..203976307hg38UCSC Ensembl
chr1:203935831..203945435hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389605
hg199605
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939770
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179102
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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