A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270588



Internal ID20837628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3253560..3254826hg38UCSC Ensembl
chr6:3253794..3255060hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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