A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv803406



Internal ID15750676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:120903520..120904383hg38UCSC Ensembl
Innerchr12:121341323..121342186hg19UCSC Ensembl
Innerchr12:119825706..119826569hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38864
hg19864
hg18864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560443
Supporting Variants
Samples
Known GenesSPPL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv803406
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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