A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245996



Internal ID20813036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58485924..58487158hg38UCSC Ensembl
chr17:56563285..56564519hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579308
Supporting Variants
Samples
Known GenesHSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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