A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701251



Internal ID15437903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56440110..56450706hg38UCSC Ensembl
Innerchr20:55015166..55025762hg19UCSC Ensembl
Innerchr20:54448573..54459169hg18UCSC Ensembl
Innerchr20:54448573..54459169hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3810597
hg1910597
hg1810597
hg1710597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525175
Supporting Variants
Samples
Known GenesCASS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701251
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