A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043665



Internal ID18786196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435409..34576796hg38UCSC Ensembl
Innerchr15:34727610..34868997hg19UCSC Ensembl
Innerchr15:32514902..32656289hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38141388
hg19141388
hg18141388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3551609
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043665
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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