A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv420n21



Internal ID20132141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37334906..37339971hg38UCSC Ensembl
chr7:37374510..37379575hg19UCSC Ensembl
chr7:37341035..37346100hg18UCSC Ensembl
chr7:37147750..37152815hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385066
hg195066
hg185066
hg175066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523409, nsv525516
Samples
Known GenesELMO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv420n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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