A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548881



Internal ID18500476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34408470..34538731hg38UCSC Ensembl
Innerchr15:34700671..34830932hg19UCSC Ensembl
Innerchr15:32487963..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38130262
hg19130262
hg18130262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050490
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)nssv3548881
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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