A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271433



Internal ID20838473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4092807..4094430hg38UCSC Ensembl
chr6:4093041..4094664hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569592
Supporting Variants
Samples
Known GenesC6orf201
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271433
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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