A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700419



Internal ID15437071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15027084..15402274hg38UCSC Ensembl
Innerchr20:15007730..15382919hg19UCSC Ensembl
Innerchr20:14955730..15330919hg18UCSC Ensembl
Innerchr20:14955730..15330919hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38375191
hg19375190
hg18375190
hg17375190
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524481
Supporting Variants
Samples
Known GenesMACROD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700419
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