A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038769



Internal ID19127988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87266138..87327258hg38UCSC Ensembl
Innerchr15:87809369..87870489hg19UCSC Ensembl
Innerchr15:85610373..85671493hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3861121
hg1961121
hg1861121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2654n100
Supporting Variantsnssv3718151
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)nsv1038769
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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