A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436601



Internal ID215214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13664779..13668894hg38UCSC Ensembl
chr3:13706279..13710394hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384116
hg194116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929525
Samples
Known GenesLINC00620
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436601
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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