A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524994



Internal ID15105601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8372105..8379130hg38UCSC Ensembl
Innerchr4:8373832..8380857hg19UCSC Ensembl
Innerchr4:8424732..8431757hg18UCSC Ensembl
Innerchr4:8491903..8498928hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg387026
hg197026
hg187026
hg177026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701025
Samples
Known GenesACOX3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524994
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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