A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552055



Internal ID16339464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101290814..101313897hg38UCSC Ensembl
Innerchr10:103050571..103073654hg19UCSC Ensembl
Innerchr10:103040561..103063644hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3823084
hg1923084
hg1823084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174570
SamplesHGDP01001
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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