A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242078



Internal ID20809118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17232429..17236642hg38UCSC Ensembl
chr17:17135743..17139956hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384214
hg194214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587108
Supporting Variants
Samples
Known GenesFLCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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