A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939196



Internal ID16233152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30382066..30417145hg38UCSC Ensembl
Innerchr20:29616742..29651821hg19UCSC Ensembl
Innerchr20:28230403..28265482hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3835080
hg1935080
hg1835080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585873
Supporting Variants
Samples
Known GenesFRG1B, MLLT10P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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