A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058271



Internal ID18800802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59844304..59931684hg38UCSC Ensembl
Innerchr20:58419359..58506739hg19UCSC Ensembl
Innerchr20:57852754..57940134hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3887381
hg1987381
hg1887381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584253
Samples
Known GenesPHACTR3, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058271
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