A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375643



Internal ID21033196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68296508..68297208hg38UCSC Ensembl
chr4:69162226..69162926hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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