A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026154



Internal ID18768686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81952009..82027249hg38UCSC Ensembl
Innerchr7:81581325..81656565hg19UCSC Ensembl
Innerchr7:81419261..81494501hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3875241
hg1975241
hg1875241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655149
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)nsv1026154
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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