A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532756



Internal ID20906117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22064303..22173770hg38UCSC Ensembl
chr20:22044941..22154408hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38109468
hg19109468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066769
Samples
Known GenesLOC100270679
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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