A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260761



Internal ID20827801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50730152..50730720hg38UCSC Ensembl
chr3:50767583..50768151hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551107
Supporting Variants
Samples
Known GenesDOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00025


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