A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268611



Internal ID20835651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118996871..118997238hg38UCSC Ensembl
chr6:119318036..119318403hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556037
Supporting Variants
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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