A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561380



Internal ID334363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14943148..14953066hg38UCSC Ensembl
chr1:15269644..15279562hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg389919
hg199919
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895858
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561380
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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