A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580679



Internal ID18878960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117211492..117373492hg38UCSC Ensembl
Innerchr2:117969068..118131068hg19UCSC Ensembl
Innerchr2:117685538..117847538hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38162001
hg19162001
hg18162001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998715
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)nssv3580679
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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