A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676779



Internal ID21198632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171502855..171503084hg38UCSC Ensembl
chr3:171220644..171220873hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676779
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.609375


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