A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552591



Internal ID15993314
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 StatusM
Merged Variantsdgv1475n54
Supporting Variantsnssv1174742, nssv1174741, nssv1174740
SamplesHGDP00784, HGDP00974, HGDP01251
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)nsv552591
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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