A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838337



Internal ID16132293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23007397..23121326hg38UCSC Ensembl
Innerchr15:22751742..22865671hg19UCSC Ensembl
Innerchr15:20303106..20417112hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38113930
hg19113930
hg18114007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568225
Supporting Variants
Samples
Known GenesTUBGCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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