A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270730



Internal ID20837770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36934518..36934993hg38UCSC Ensembl
chr6:36902294..36902769hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270730
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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