A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038537



Internal ID19127756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32565269hg38UCSC Ensembl
Innerchr15:32539525..32857470hg19UCSC Ensembl
Innerchr15:30326817..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38317946
hg19317946
hg18317946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3547816, nssv3547817, nssv3547819, nssv3547818
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)nsv1038537
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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