A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263949



Internal ID20830989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64997481..65003509hg38UCSC Ensembl
chr3:64983156..64989184hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg386029
hg196029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541800
Supporting Variants
Samples
Known GenesADAMTS9-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00034


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