A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256693



Internal ID20823733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:122700474..122701627hg38UCSC Ensembl
chr2:123458050..123459203hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg381154
hg191154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00027


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