A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245338



Internal ID20812378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56655411..56656293hg38UCSC Ensembl
chr18:54322642..54323524hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589499
Supporting Variants
Samples
Known GenesWDR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245338
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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