A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245324



Internal ID20812364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56204291..56204794hg38UCSC Ensembl
chr17:54281652..54282155hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594206
Supporting Variants
Samples
Known GenesANKFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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