A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356054



Internal ID21013607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133598920..133602577hg38UCSC Ensembl
chr3:133317764..133321421hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg383658
hg193658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094800
Samples
Known GenesTOPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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