A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541199



Internal ID20914483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58140701..58142500hg38UCSC Ensembl
chr20:56715757..56717556hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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