A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244615



Internal ID20811655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75387555..75388100hg38UCSC Ensembl
chr17:73383636..73384181hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592060
Supporting Variants
Samples
Known GenesGRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244615
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