A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454641



Internal ID232737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40203706..40203761hg38UCSC Ensembl
chr4:40205326..40205381hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948107
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454641
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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