A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538363



Internal ID20911680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45343150..45344606hg38UCSC Ensembl
chr20:43971790..43973246hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381457
hg191457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068334
Samples
Known GenesSDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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