A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523767



Internal ID15104374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45097023..45097609hg38UCSC Ensembl
Innerchr3:45138515..45139101hg19UCSC Ensembl
Innerchr3:45113519..45114105hg18UCSC Ensembl
Innerchr3:45113519..45114105hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38587
hg19587
hg18587
hg17587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699588
Samples
Known GenesCDCP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523767
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer