A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691557



Internal ID21213410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32974269..32974396hg38UCSC Ensembl
chr1:33439870..33439997hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801192
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691557
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.2


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