A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996538



Internal ID21905881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178809644..179180014hg38UCSC Ensembl
chr4:179730798..180101168hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38370371
hg19370371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996538
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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