A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037332



Internal ID18779863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430589..34582282hg38UCSC Ensembl
Innerchr15:34722790..34874483hg19UCSC Ensembl
Innerchr15:32510082..32661775hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38151694
hg19151694
hg18151694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3549694
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)nsv1037332
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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