A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685574



Internal ID21207411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113046441..113046490hg38UCSC Ensembl
chr3:112765288..112765337hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685574
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.603448


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