A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048724



Internal ID19137943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25445557..25464586hg38UCSC Ensembl
Innerchr15:25690704..25709733hg19UCSC Ensembl
Innerchr15:23241797..23260826hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3819030
hg1919030
hg1819030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545630
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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