A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244603



Internal ID20811643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75175622..75176527hg38UCSC Ensembl
chr17:73171717..73172622hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582744
Supporting Variants
Samples
Known GenesSUMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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