A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891546



Internal ID22666586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24806472..24809714hg38UCSC Ensembl
chr6:24806700..24809942hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435975
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891546
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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