A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243148



Internal ID20810188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61632472..61638728hg38UCSC Ensembl
chr17:59709833..59716089hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg386257
hg196257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243148
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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