A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585957



Internal ID16373366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37364924..37442038hg38UCSC Ensembl
Innerchr20:35993327..36070440hg19UCSC Ensembl
Innerchr20:35426741..35503854hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3877115
hg1977114
hg1877114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7566n54
Supporting Variantsnssv1151352
SamplesHGDP00850
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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