A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274852



Internal ID20841892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87241089..87241689hg38UCSC Ensembl
chr6:87950807..87951407hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558311
Supporting Variants
Samples
Known GenesZNF292
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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