A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532789



Internal ID20906150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9482237..9482860hg38UCSC Ensembl
chr20:9462884..9463507hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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