A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941799



Internal ID16235755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58890396..58892021hg38UCSC Ensembl
Innerchr20:57465451..57467076hg19UCSC Ensembl
Innerchr20:56898846..56900471hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381626
hg191626
hg181626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586357
Supporting Variants
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941799
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