A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274071



Internal ID20841111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73344382..73345321hg38UCSC Ensembl
chr6:74054105..74055044hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274071
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer