A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506519



Internal ID18458114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133429369..133535560hg38UCSC Ensembl
Innerchr10:135242873..135349064hg19UCSC Ensembl
Innerchr10:135092863..135199054hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38106192
hg19106192
hg18106192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042246
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)nssv3506519
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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