A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551924



Internal ID15992647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92452985..92530727hg38UCSC Ensembl
Innerchr10:94212742..94290484hg19UCSC Ensembl
Innerchr10:94202722..94280464hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3877743
hg1977743
hg1877743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1349n54
Supporting Variantsnssv753957
Samples
Known GenesIDE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551924
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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