A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509447



Internal ID18461042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17006669..17549229hg38UCSC Ensembl
Innerchr10:17048668..17591228hg19UCSC Ensembl
Innerchr10:17088674..17631234hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38542561
hg19542561
hg18542561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039697
Supporting Variants
Samples
Known GenesCUBN, ST8SIA6, ST8SIA6-AS1, TRDMT1, VIM, VIM-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509447
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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