A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586534



Internal ID16373943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62954354..62968122hg38UCSC Ensembl
Innerchr20:61585706..61599474hg19UCSC Ensembl
Innerchr20:61056151..61069919hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3813769
hg1913769
hg1813769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7659n54
Supporting Variantsnssv1152395
Samples1780862021_A
Known GenesSLC17A9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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