A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053572



Internal ID19142791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76161853..76193625hg38UCSC Ensembl
Innerchr15:76454194..76485966hg19UCSC Ensembl
Innerchr15:74241249..74273021hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3831773
hg1931773
hg1831773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2625n100
Supporting Variantsnssv3553738, nssv3553736, nssv3553735, nssv3553737, nssv3553739
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)nsv1053572
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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