A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894629



Internal ID22669703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163397251..163399188hg38UCSC Ensembl
chr4:164318403..164320340hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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