A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525129



Internal ID15452422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178958584..178963236hg38UCSC Ensembl
Innerchr5:178385585..178390237hg19UCSC Ensembl
Innerchr5:178318191..178322843hg18UCSC Ensembl
Innerchr5:178318191..178322843hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384653
hg194653
hg184653
hg174653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701197
Samples
Known GenesZNF454
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525129
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