A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607697



Internal ID16048420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:82196750..82222281hg38UCSC Ensembl
Innerchr7:81826066..81851597hg19UCSC Ensembl
Innerchr7:81664002..81689533hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3825532
hg1925532
hg1825532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089229
Samples
Known GenesCACNA2D1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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