A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551913



Internal ID16339322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91441834..91448214hg38UCSC Ensembl
Innerchr10:93201591..93207971hg19UCSC Ensembl
Innerchr10:93191571..93197951hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg386381
hg196381
hg186381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753454
Samples
Known GenesHECTD2, LOC100188947
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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