A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244430



Internal ID20811470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32349005..32349527hg38UCSC Ensembl
chr17:30676024..30676546hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244430
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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