A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv365n21



Internal ID22766557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181087652..181151750hg38UCSC Ensembl
chr5:180514652..180578750hg19UCSC Ensembl
chr5:180447258..180511356hg18UCSC Ensembl
chr5:180447258..180511356hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3864099
hg1964099
hg1864099
hg1764099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524116, nsv523076
Samples
Known GenesOR2V1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv365n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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