A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271446



Internal ID20838486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4169872..4174777hg38UCSC Ensembl
chr6:4170106..4175011hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384906
hg194906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271446
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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