A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898299



Internal ID22673412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83077289..83077630hg38UCSC Ensembl
chr4:83998442..83998783hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898299
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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