A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv468n21



Internal ID22766660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106805428..106810920hg38UCSC Ensembl
chr8:107817656..107823148hg19UCSC Ensembl
chr8:107886832..107892324hg18UCSC Ensembl
chr8:107886832..107892324hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg385493
hg195493
hg185493
hg175493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523126, nsv516791
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv468n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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