A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518905



Internal ID15446198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63221277..63264557hg38UCSC Ensembl
Innerchr20:61852629..61895909hg19UCSC Ensembl
Innerchr20:61323074..61366354hg18UCSC Ensembl
Innerchr20:61323074..61366354hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3843281
hg1943281
hg1843281
hg1743281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696363
Samples
Known GenesBIRC7, FLJ16779, MIR3196, NKAIN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518905
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