A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662561



Internal ID15399213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5311440..5317338hg38UCSC Ensembl
Innerchr20:5292086..5297984hg19UCSC Ensembl
Innerchr20:5240086..5245984hg18UCSC Ensembl
Innerchr20:5240086..5245984hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg385899
hg195899
hg185899
hg175899
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515639
Supporting Variants
Samples
Known GenesPROKR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662561
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