A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024460



Internal ID18766992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81937185..81981408hg38UCSC Ensembl
Innerchr7:81566501..81610724hg19UCSC Ensembl
Innerchr7:81404437..81448660hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3844224
hg1944224
hg1844224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655148
Samples
Known GenesCACNA2D1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024460
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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