A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045863



Internal ID18788394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2126462..2151588hg38UCSC Ensembl
Innerchr12:2235628..2260754hg19UCSC Ensembl
Innerchr12:2105889..2131015hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3825127
hg1925127
hg1825127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1339n100
Supporting Variantsnssv3517518
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)nsv1045863
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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