A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033925



Internal ID18776459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:82243429..82299207hg38UCSC Ensembl
Innerchr7:81872745..81928523hg19UCSC Ensembl
Innerchr7:81710681..81766459hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3855779
hg1955779
hg1855779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655151
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)nsv1033925
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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