A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585987



Internal ID16026710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41254935..41257465hg38UCSC Ensembl
Innerchr20:39883575..39886105hg19UCSC Ensembl
Innerchr20:39316989..39319519hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg382531
hg192531
hg182531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7571n54
Supporting Variantsnssv939412, nssv939409, nssv939408, nssv939411, nssv939414, nssv939410, nssv939413
Samples
Known GenesZHX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585987
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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