A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940863



Internal ID15888133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45722456..45749938hg38UCSC Ensembl
Innerchr20:44351095..44378577hg19UCSC Ensembl
Innerchr20:43784509..43811984hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3827483
hg1927483
hg1827476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586125
Supporting Variants
Samples
Known GenesSPINT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940863
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