A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv401n21



Internal ID20132122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2600507..2714033hg38UCSC Ensembl
chr7:2640141..2753667hg19UCSC Ensembl
chr7:2606667..2720193hg18UCSC Ensembl
chr7:2413382..2526908hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38113527
hg19113527
hg18113527
hg17113527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518027, nsv517403
Samples
Known GenesAMZ1, IQCE, TTYH3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv401n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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