A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256414



Internal ID20823454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202245203..202245575hg38UCSC Ensembl
chr2:203109926..203110298hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256414
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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