A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3708070



Internal ID18659665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2136684..2161113hg38UCSC Ensembl
Innerchr12:2245850..2270279hg19UCSC Ensembl
Innerchr12:2116111..2140540hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3824430
hg1924430
hg1824430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043538
Supporting Variants
Samples
Known GenesCACNA1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3708070
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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