A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268595



Internal ID20835635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117681911..117682391hg38UCSC Ensembl
chr6:118003074..118003554hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568344
Supporting Variants
Samples
Known GenesNUS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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