A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548869



Internal ID20922047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58383442..58386788hg38UCSC Ensembl
chr20:56958498..56961844hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg383347
hg193347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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