A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406072



Internal ID21063625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18461757..18462337hg38UCSC Ensembl
chr6:18461988..18462568hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143065
Samples
Known GenesRNF144B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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