A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101534



Internal ID20668574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64884125..64884656hg38UCSC Ensembl
chr3:64869800..64870331hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365121
Supporting Variants
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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