A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174579



Internal ID15508687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125621256..125726016hg38UCSC Ensembl
Innerchr10:127309825..127414585hg19UCSC Ensembl
Innerchr10:127299815..127404575hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38104761
hg19104761
hg18104761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552293
Supporting Variants
Samples1780862576_A
Known GenesC10orf137, FLJ37035, LOC283038, TEX36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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