A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559398



Internal ID332433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64606594..64681966hg38UCSC Ensembl
chr3:64592270..64667642hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3875373
hg1975373
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933927
Samples
Known GenesADAMTS9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559398
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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