A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044924



Internal ID19134143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32257489..32584771hg38UCSC Ensembl
Innerchr15:32549690..32876972hg19UCSC Ensembl
Innerchr15:30336982..30664264hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38327283
hg19327283
hg18327283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3721654, nssv3547858, nssv3547859, nssv3547857
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044924
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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