A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101514



Internal ID20668554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64677383..64678473hg38UCSC Ensembl
chr3:64663059..64664149hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362879
Supporting Variants
Samples
Known GenesADAMTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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