A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150955



Internal ID15508211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45842587..45880235hg38UCSC Ensembl
Innerchr20:44471226..44508874hg19UCSC Ensembl
Innerchr20:43904633..43942281hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3837649
hg1937649
hg1837649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586133
Supporting Variants
Samples1780862380_A
Known GenesACOT8, SNX21, ZSWIM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150955
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