A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786605



Internal ID15733875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2137854..2146161hg38UCSC Ensembl
Innerchr12:2247020..2255327hg19UCSC Ensembl
Innerchr12:2117281..2125588hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg388308
hg198308
hg188308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557057
Supporting Variants
Samples
Known GenesCACNA1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv786605
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer