A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525955



Internal ID15106562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75439434..75594447hg38UCSC Ensembl
Innerchr16:75473332..75628345hg19UCSC Ensembl
Innerchr16:74030833..74185846hg18UCSC Ensembl
Innerchr16:74030833..74185846hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38155014
hg19155014
hg18155014
hg17155014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702163
Samples
Known GenesCHST5, CHST6, GABARAPL2, TMEM170A, TMEM231
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525955
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