A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494038



Internal ID22551968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64547120..64550218hg38UCSC Ensembl
chr3:64532796..64535894hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg383099
hg193099
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836451
Supporting Variants
Samples
Known GenesADAMTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494038
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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