A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701025



Internal ID15090991
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524994
Supporting Variants
Samples
Known GenesACOX3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701025
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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