A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700217



Internal ID15090183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:82405705..82809418hg38UCSC Ensembl
Innerchr7:82035021..82438734hg19UCSC Ensembl
Innerchr7:81872957..82276670hg18UCSC Ensembl
Innerchr7:81679672..82083385hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38403714
hg19403714
hg18403714
hg17403714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524315
Supporting Variants
Samples
Known GenesCACNA2D1, PCLO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700217
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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