A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692635



Internal ID21214485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71260247..71260739hg38UCSC Ensembl
chr2:71487377..71487869hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692635
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.046875


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