A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560645



Internal ID333648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174452057..174457988hg38UCSC Ensembl
chr3:174169847..174175778hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg385932
hg195932
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560645
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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