A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535791



Internal ID20909144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63898687..63922983hg38UCSC Ensembl
chr20:62530040..62554336hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3824297
hg1924297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070276
Samples
Known GenesDNAJC5, MIR941-1, MIR941-2, MIR941-3, MIR941-4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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