A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580875



Internal ID18879156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131956759..132057995hg38UCSC Ensembl
Innerchr2:132714332..132815568hg19UCSC Ensembl
Innerchr2:132430802..132532038hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg38101237
hg19101237
hg18101237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012896
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)nssv3580875
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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