A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271517



Internal ID20838557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53323577..53324008hg38UCSC Ensembl
chr6:53188375..53188806hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569307
Supporting Variants
Samples
Known GenesELOVL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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