A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058633



Internal ID18801164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46433755..46492168hg38UCSC Ensembl
Innerchr20:45062394..45120807hg19UCSC Ensembl
Innerchr20:44495801..44554214hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3858414
hg1958414
hg1858414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584943
Samples
Known GenesMKRN7P, ZNF663P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058633
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer