A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801999



Internal ID15749269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110274407..110281536hg38UCSC Ensembl
Innerchr12:110712212..110719341hg19UCSC Ensembl
Innerchr12:109196595..109203724hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg387130
hg197130
hg187130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560152
Supporting Variants
Samples
Known GenesATP2A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801999
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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