A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580893



Internal ID18879174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34047201..34125506hg38UCSC Ensembl
Innerchr2:34272268..34350573hg19UCSC Ensembl
Innerchr2:34125772..34204077hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3878306
hg1978306
hg1878306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009928
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)nssv3580893
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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