A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436861



Internal ID215469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177286944..177295834hg38UCSC Ensembl
chr3:177004732..177013622hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg388891
hg198891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv359n206
Supporting Variantsnssv16943572
Samples
Known GenesLINC00501
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436861
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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