A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900518



Internal ID22675661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145622530..145623403hg38UCSC Ensembl
chr6:145943666..145944539hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900518
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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