A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557060



Internal ID15997783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2137854..2149783hg38UCSC Ensembl
Innerchr12:2247020..2258949hg19UCSC Ensembl
Innerchr12:2117281..2129210hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3811930
hg1911930
hg1811930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2287n54
Supporting Variantsnssv786618
Samples
Known GenesCACNA1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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