A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536606



Internal ID20909952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57680654..57683201hg38UCSC Ensembl
chr20:56255710..56258257hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069086
Samples
Known GenesPMEPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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