A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585988



Internal ID16026711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41255667..41257465hg38UCSC Ensembl
Innerchr20:39884307..39886105hg19UCSC Ensembl
Innerchr20:39317721..39319519hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7571n54
Supporting Variantsnssv939417, nssv939415, nssv939416, nssv939418, nssv939419
Samples
Known GenesZHX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585988
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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