A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940864



Internal ID15888134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45723267..45734110hg38UCSC Ensembl
Innerchr20:44351906..44362749hg19UCSC Ensembl
Innerchr20:43785320..43796156hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810844
hg1910844
hg1810837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586126
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)nssv940864
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