A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052694



Internal ID19141913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70680702..70746740hg38UCSC Ensembl
Innerchr15:70973041..71039079hg19UCSC Ensembl
Innerchr15:68760095..68826133hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3866039
hg1966039
hg1866039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553675
Samples
Known GenesUACA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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