A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503692



Internal ID18455287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73901953..73946795hg38UCSC Ensembl
Innerchr10:75661711..75706553hg19UCSC Ensembl
Innerchr10:75331717..75376559hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3844843
hg1944843
hg1844843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035390
Supporting Variants
Samples
Known GenesC10orf55, PLAU
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503692
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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