A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555221



Internal ID20928312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53153274..53166232hg38UCSC Ensembl
chr20:51769813..51782771hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3812959
hg1912959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068239
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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