A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542965



Internal ID20916216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59422438..59433041hg38UCSC Ensembl
chr20:57997493..58008096hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3810604
hg1910604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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