A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101533



Internal ID20668573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64878108..64878508hg38UCSC Ensembl
chr3:64863783..64864183hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374310
Supporting Variants
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00084


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