A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563188



Internal ID336125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142329359..142329372hg38UCSC Ensembl
chr5:141708924..141708937hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3814
hg1914
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563188
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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