A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551476



Internal ID16338885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69710213..69728284hg38UCSC Ensembl
Innerchr10:71469969..71488040hg19UCSC Ensembl
Innerchr10:71139975..71158046hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3818072
hg1918072
hg1818072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174246
SamplesHGDP00330
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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