A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047554



Internal ID18790085
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 StatusM
Merged Variantsdgv701n100
Supporting Variantsnssv3518763
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)nsv1047554
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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