A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555582



Internal ID328736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69977138..69977185hg38UCSC Ensembl
chr15:70269477..70269524hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3848
hg1948
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555582
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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