A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549684



Internal ID18501279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430589..34565797hg38UCSC Ensembl
Innerchr15:34722790..34857998hg19UCSC Ensembl
Innerchr15:32510082..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135209
hg19135209
hg18135209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041232
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3549684
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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