A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245236



Internal ID20812276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5161926..5162428hg38UCSC Ensembl
chr17:5065221..5065723hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588163
Supporting Variants
Samples
Known GenesUSP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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