A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741053



Internal ID20517030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178959609..178964130hg38UCSC Ensembl
chr5:178386610..178391131hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384522
hg194522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295924
Samples
Known GenesZNF454
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741053
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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