A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550389



Internal ID16337798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33862464..33873549hg38UCSC Ensembl
Innerchr10:34151392..34162477hg19UCSC Ensembl
Innerchr10:34191398..34202483hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811086
hg1911086
hg1811086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv746835
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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