A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256386



Internal ID20823426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201476694..201477058hg38UCSC Ensembl
chr2:202341417..202341781hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550799
Supporting Variants
Samples
Known GenesSTRADB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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