A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551329



Internal ID20924466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48784250..48788874hg38UCSC Ensembl
chr20:47400787..47405411hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg384625
hg194625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068950
Samples
Known GenesPREX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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