A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580286



Internal ID18878567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117021251..117166577hg38UCSC Ensembl
Innerchr2:117778827..117924153hg19UCSC Ensembl
Innerchr2:117495297..117640623hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38145327
hg19145327
hg18145327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005839
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)nssv3580286
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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