A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268501



Internal ID20835541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111698262..111698778hg38UCSC Ensembl
chr6:112019465..112019981hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573365
Supporting Variants
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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