A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245946



Internal ID20812986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56428155..56428748hg38UCSC Ensembl
chr17:54505516..54506109hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582351
Supporting Variants
Samples
Known GenesANKFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245946
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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