A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585955



Internal ID16373364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37340671..37423443hg38UCSC Ensembl
Innerchr20:35969074..36051846hg19UCSC Ensembl
Innerchr20:35402488..35485260hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3882773
hg1982773
hg1882773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7565n54
Supporting Variantsnssv939351
Samples
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585955
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