A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv436n21



Internal ID18990909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:151125105..151135826hg38UCSC Ensembl
chr7:150822192..150832913hg19UCSC Ensembl
chr7:150453125..150463846hg18UCSC Ensembl
chr7:150259840..150270561hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3810722
hg1910722
hg1810722
hg1710722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523930, nsv528732
Samples
Known GenesAGAP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv436n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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