A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996764



Internal ID21906107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26467888..26467958hg38UCSC Ensembl
chr4:26469510..26469580hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996764
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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