A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261677



Internal ID20828717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98301369..98323207hg38UCSC Ensembl
chr2:98917832..98939670hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3821839
hg1921839
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541664
Supporting Variants
Samples
Known GenesVWA3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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