A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789954



Internal ID15737224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27495478..27504092hg38UCSC Ensembl
Innerchr12:27648411..27657025hg19UCSC Ensembl
Innerchr12:27539678..27548292hg18UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg388615
hg198615
hg188615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557814
Supporting Variants
Samples
Known GenesSMCO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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