A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv803880



Internal ID15751150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:123911640..123915714hg38UCSC Ensembl
Innerchr12:124396187..124400261hg19UCSC Ensembl
Innerchr12:122962140..122966214hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384075
hg194075
hg184075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560531
Supporting Variants
Samples
Known GenesDNAH10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv803880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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