A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261760



Internal ID20828800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120087528..120087901hg38UCSC Ensembl
chr3:119806375..119806748hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555688
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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