A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585991



Internal ID16026714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41278374..41278591hg38UCSC Ensembl
Innerchr20:39907014..39907231hg19UCSC Ensembl
Innerchr20:39340428..39340645hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38218
hg19218
hg18218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939437, nssv939441, nssv939434, nssv939440, nssv939439, nssv939435, nssv939432, nssv939438, nssv939431, nssv939433, nssv939430, nssv939442, nssv939436
Samples
Known GenesZHX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585991
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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