A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525956



Internal ID15453249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16612514..16620874hg38UCSC Ensembl
Innerchr20:16593159..16601519hg19UCSC Ensembl
Innerchr20:16541159..16549519hg18UCSC Ensembl
Innerchr20:16541159..16549519hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg388361
hg198361
hg188361
hg178361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702165
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525956
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