A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036796



Internal ID18779327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2136938..2150789hg38UCSC Ensembl
Innerchr12:2246104..2259955hg19UCSC Ensembl
Innerchr12:2116365..2130216hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3813852
hg1913852
hg1813852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1341n100
Supporting Variantsnssv3522436, nssv3504043
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)nsv1036796
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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