A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515466



Internal ID18467061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86460173..86577343hg38UCSC Ensembl
Innerchr10:88219930..88337100hg19UCSC Ensembl
Innerchr10:88209910..88327080hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38117171
hg19117171
hg18117171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045699
Supporting Variants
Samples
Known GenesWAPAL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515466
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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