A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274859



Internal ID20841899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87454797..87455105hg38UCSC Ensembl
chr6:88164515..88164823hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558656
Supporting Variants
Samples
Known GenesC6orf165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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