A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271960



Internal ID20839000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134933803..134934888hg38UCSC Ensembl
chr6:135254941..135256026hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557484
Supporting Variants
Samples
Known GenesALDH8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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