A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721655



Internal ID19019936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32274298..32567645hg38UCSC Ensembl
Innerchr15:32566499..32859846hg19UCSC Ensembl
Innerchr15:30353791..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38293348
hg19293348
hg18293348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050930
Supporting Variants
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)nssv3721655
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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