A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471191



Internal ID248935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107383458..107383581hg38UCSC Ensembl
chr4:108304615..108304738hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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