A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258286



Internal ID20825326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69365262..69365842hg38UCSC Ensembl
chr2:69592394..69592974hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537165
Supporting Variants
Samples
Known GenesGFPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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