A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527925



Internal ID15455218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2243138..2305739hg38UCSC Ensembl
Innerchr4:2244865..2307466hg19UCSC Ensembl
Innerchr4:2214663..2277264hg18UCSC Ensembl
Innerchr4:2212096..2274697hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3862602
hg1962602
hg1862602
hg1762602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv312n21
Supporting Variantsnssv704432
Samples
Known GenesMIR4800, MXD4, ZFYVE28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527925
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