A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv473n21



Internal ID22766665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136497229..136498260hg38UCSC Ensembl
chr8:137509472..137510503hg19UCSC Ensembl
chr8:137578654..137579685hg18UCSC Ensembl
chr8:137578654..137579685hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381032
hg191032
hg181032
hg171032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522867, nsv520473
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv473n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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