A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517438



Internal ID15444731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1178828..1180419hg38UCSC Ensembl
Innerchr20:1159472..1161063hg19UCSC Ensembl
Innerchr20:1107472..1109063hg18UCSC Ensembl
Innerchr20:1107472..1109063hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381592
hg191592
hg181592
hg171592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656010, nssv667252, nssv681646, nssv681802, nssv652018
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517438
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer