A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262118



Internal ID20829158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48044105..48045185hg38UCSC Ensembl
chr3:48085595..48086675hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542401
Supporting Variants
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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