A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580897



Internal ID18879178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34427331..34502788hg38UCSC Ensembl
Innerchr2:34652398..34727855hg19UCSC Ensembl
Innerchr2:34505902..34581359hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3875458
hg1975458
hg1875458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005622
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)nssv3580897
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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