A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532715



Internal ID20906076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5180378..5181073hg38UCSC Ensembl
chr20:5161024..5161719hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068138
Samples
Known GenesCDS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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