A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550385



Internal ID16337794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32900564..32901564hg38UCSC Ensembl
Innerchr10:33189492..33190492hg19UCSC Ensembl
Innerchr10:33229498..33230498hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1031n54
Supporting Variantsnssv746829
Samples
Known GenesITGB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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