A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585931



Internal ID16026654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34654522..34654732hg38UCSC Ensembl
Innerchr20:33242326..33242536hg19UCSC Ensembl
Innerchr20:32705987..32706197hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38211
hg19211
hg18211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939299, nssv939295, nssv939307, nssv939302, nssv939305, nssv939296, nssv939304, nssv939297, nssv939306, nssv939298, nssv939303, nssv939300, nssv939301
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585931
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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