A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048760



Internal ID18791291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76042203..76204636hg38UCSC Ensembl
Innerchr15:76334544..76496977hg19UCSC Ensembl
Innerchr15:74121599..74284032hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38162434
hg19162434
hg18162434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553702
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)nsv1048760
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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