A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786519



Internal ID15733789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2127676..2148329hg38UCSC Ensembl
Innerchr12:2236842..2257495hg19UCSC Ensembl
Innerchr12:2107103..2127756hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3820654
hg1920654
hg1820654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557042
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)nssv786519
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