A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943761



Internal ID16237717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63576509..63617922hg38UCSC Ensembl
Innerchr20:62207862..62249275hg19UCSC Ensembl
Innerchr20:61678306..61719719hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3841414
hg1941414
hg1841414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586582
Supporting Variants
Samples
Known GenesGMEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943761
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