A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896016



Internal ID22671105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89841068..89841266hg38UCSC Ensembl
chr4:90762219..90762417hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418009
Samples
Known GenesLOC644248
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896016
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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