A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255733



Internal ID20822773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101334393..101334891hg38UCSC Ensembl
chr2:101950855..101951353hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255733
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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