A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256755



Internal ID20823795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:126589460..126624076hg38UCSC Ensembl
chr2:127347037..127381653hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3834617
hg1934617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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