A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244676



Internal ID20811716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54156680..54157409hg38UCSC Ensembl
chr18:51683050..51683779hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581925
Supporting Variants
Samples
Known GenesMBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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