A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551537



Internal ID15992260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76127736..76170678hg38UCSC Ensembl
Innerchr10:77887494..77930436hg19UCSC Ensembl
Innerchr10:77557500..77600442hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3842943
hg1942943
hg1842943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750295
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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