A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260758



Internal ID20827798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50693560..50694271hg38UCSC Ensembl
chr3:50730991..50731702hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538832
Supporting Variants
Samples
Known GenesDOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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