A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256402



Internal ID20823442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202080508..202081623hg38UCSC Ensembl
chr2:202945231..202946346hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540343
Supporting Variants
Samples
Known GenesLOC100652824
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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