A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468626



Internal ID246421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100760555..100760672hg38UCSC Ensembl
chr4:101681712..101681829hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468626
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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