A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655152



Internal ID18606747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:82328229..82827828hg38UCSC Ensembl
Innerchr7:81957545..82457144hg19UCSC Ensembl
Innerchr7:81795481..82295080hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38499600
hg19499600
hg18499600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027670
Supporting Variants
Samples
Known GenesCACNA2D1, PCLO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655152
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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