A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540266



Internal ID20913558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57310631..57321093hg38UCSC Ensembl
chr20:55885687..55896149hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3810463
hg1910463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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