A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542478



Internal ID20915737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53133701..53134600hg38UCSC Ensembl
chr20:51750240..51751139hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068238
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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