A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558591



Internal ID331650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157566094..157566127hg38UCSC Ensembl
chr5:156993102..156993135hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3834
hg1934
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975956
Samples
Known GenesADAM19
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558591
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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