A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580297



Internal ID18878578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117021251..117175135hg38UCSC Ensembl
Innerchr2:117778827..117932711hg19UCSC Ensembl
Innerchr2:117495297..117649181hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38153885
hg19153885
hg18153885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005141
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)nssv3580297
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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