A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938977



Internal ID16232933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25786711..25876293hg38UCSC Ensembl
Innerchr20:25767347..25856929hg19UCSC Ensembl
Innerchr20:25715347..25804929hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3889583
hg1989583
hg1889583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585749
Supporting Variants
Samples
Known GenesFAM182B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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