A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583087



Internal ID18881368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:179069463..179098536hg38UCSC Ensembl
Innerchr2:179934190..179963263hg19UCSC Ensembl
Innerchr2:179642435..179671508hg18UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3829074
hg1929074
hg1829074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003301
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583087
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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