A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524925



Internal ID15452218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25277366..25294382hg38UCSC Ensembl
Innerchr4:25278988..25296004hg19UCSC Ensembl
Innerchr4:24888086..24905102hg18UCSC Ensembl
Innerchr4:24955257..24972273hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3817017
hg1917017
hg1817017
hg1717017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700938
Samples
Known GenesPI4K2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524925
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