A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260903



Internal ID20827943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85315940..85343854hg38UCSC Ensembl
chr2:85543063..85570977hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3827915
hg1927915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550543
Supporting Variants
Samples
Known GenesRETSAT, TGOLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01858


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