A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054713



Internal ID19143932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76168121..76213565hg38UCSC Ensembl
Innerchr15:76460462..76505906hg19UCSC Ensembl
Innerchr15:74247517..74292961hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3845445
hg1945445
hg1845445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553743
Samples
Known GenesC15orf27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054713
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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