A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243394



Internal ID20810434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9598473..9599943hg38UCSC Ensembl
chr17:9501790..9503260hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381471
hg191471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584758
Supporting Variants
Samples
Known GenesWDR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243394
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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