A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274886



Internal ID20841926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87843930..87844686hg38UCSC Ensembl
chr6:88553648..88554404hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00031


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