A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550327



Internal ID15991050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30868788..31276426hg38UCSC Ensembl
Innerchr10:31157717..31565355hg19UCSC Ensembl
Innerchr10:31197723..31605361hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38407639
hg19407639
hg18407639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv745715
Samples
Known GenesZNF438
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550327
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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