A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509286



Internal ID18460881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16385108..16530259hg38UCSC Ensembl
Innerchr10:16427107..16572258hg19UCSC Ensembl
Innerchr10:16467113..16612264hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38145152
hg19145152
hg18145152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046833
Supporting Variants
Samples
Known GenesC1QL3, PTER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509286
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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