A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174742



Internal ID15532057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133272250..133333210hg38UCSC Ensembl
Innerchr10:135085754..135146714hg19UCSC Ensembl
Innerchr10:134935744..134996704hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3860961
hg1960961
hg1860961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552591
Supporting Variants
SamplesHGDP01251
Known GenesADAM8, CALY, TUBGCP2, ZNF511
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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