A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544913



Internal ID20918151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60772788..60779596hg38UCSC Ensembl
chr20:59347844..59354652hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386809
hg196809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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