A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703326



Internal ID15093292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14014568..14075301hg38UCSC Ensembl
Innerchr20:13995214..14055947hg19UCSC Ensembl
Innerchr20:13943214..14003947hg18UCSC Ensembl
Innerchr20:13943214..14003947hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3860734
hg1960734
hg1860734
hg1760734
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526954
Supporting Variants
Samples
Known GenesMACROD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703326
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