A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244460



Internal ID20811500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33424896..33425851hg38UCSC Ensembl
chr17:31751914..31752869hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576423
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244460
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