A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706278



Internal ID18657873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133429369..133552598hg38UCSC Ensembl
Innerchr10:135242873..135366102hg19UCSC Ensembl
Innerchr10:135092863..135216092hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38123230
hg19123230
hg18123230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042575
Supporting Variants
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706278
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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