A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039334



Internal ID18781865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34427734..34538731hg38UCSC Ensembl
Innerchr15:34719935..34830932hg19UCSC Ensembl
Innerchr15:32507227..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38110998
hg19110998
hg18110998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2557n100
Supporting Variantsnssv3549402, nssv3549403
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)nsv1039334
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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