A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244445



Internal ID20811485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32475624..32476260hg38UCSC Ensembl
chr17:30802642..30803278hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580471
Supporting Variants
Samples
Known GenesPSMD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244445
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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