A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580891



Internal ID18879172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34013902..34093335hg38UCSC Ensembl
Innerchr2:34238969..34318402hg19UCSC Ensembl
Innerchr2:34092473..34171906hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3879434
hg1979434
hg1879434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011569
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)nssv3580891
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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