A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550788



Internal ID20923928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50741194..50744413hg38UCSC Ensembl
chr20:49357731..49360950hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383220
hg193220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067676
Samples
Known GenesPARD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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