A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547854



Internal ID18846135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32257489..32567645hg38UCSC Ensembl
Innerchr15:32549690..32859846hg19UCSC Ensembl
Innerchr15:30336982..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38310157
hg19310157
hg18310157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048076
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)nssv3547854
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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