A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718068



Internal ID19016349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76586021..76610843hg38UCSC Ensembl
Innerchr15:76878362..76903184hg19UCSC Ensembl
Innerchr15:74665417..74690239hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3824823
hg1924823
hg1824823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053005
Supporting Variants
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718068
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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