A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550382



Internal ID16337791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31366839..31500787hg38UCSC Ensembl
Innerchr10:31655768..31789715hg19UCSC Ensembl
Innerchr10:31695774..31829721hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38133949
hg19133948
hg18133948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv746825
Samples
Known GenesZEB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550382
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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