A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518763



Internal ID18470358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31324455..31388389hg38UCSC Ensembl
Innerchr10:31613384..31677318hg19UCSC Ensembl
Innerchr10:31653390..31717324hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3863935
hg1963935
hg1863935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047554
Supporting Variants
Samples
Known GenesZEB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518763
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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