A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551684



Internal ID18503279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34439042..34538731hg38UCSC Ensembl
Innerchr15:34731243..34830932hg19UCSC Ensembl
Innerchr15:32518535..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3899690
hg1999690
hg1899690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040063
Supporting Variants
Samples
Known GenesGOLGA8B, 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)nssv3551684
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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