A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547796



Internal ID18499391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32196661..32550909hg38UCSC Ensembl
Innerchr15:32488862..32843110hg19UCSC Ensembl
Innerchr15:30276154..30630402hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38354249
hg19354249
hg18354249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048426
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)nssv3547796
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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