A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045565



Internal ID19134784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85798051..85812809hg38UCSC Ensembl
Innerchr15:86341282..86356040hg19UCSC Ensembl
Innerchr15:84142286..84157044hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3814759
hg1914759
hg1814759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2653n100
Supporting Variantsnssv3555091
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)nsv1045565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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