A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244565



Internal ID20811605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73077965..73078788hg38UCSC Ensembl
chr17:71074104..71074927hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576806
Supporting Variants
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244565
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