A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260573



Internal ID20827613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184031081..184032164hg38UCSC Ensembl
chr3:183748869..183749952hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574156
Supporting Variants
Samples
Known GenesHTR3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260573
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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