A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522895



Internal ID20896256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4225704..4227804hg38UCSC Ensembl
chr20:4206351..4208451hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382101
hg192101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067652
Samples
Known GenesADRA1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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