A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550213



Internal ID15990936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:23193706..23334594hg38UCSC Ensembl
Innerchr10:23482635..23623523hg19UCSC Ensembl
Innerchr10:23522641..23663529hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38140889
hg19140889
hg18140889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744715
Samples
Known GenesC10orf115, C10orf67, PTF1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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