A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242969



Internal ID20810009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41398485..41399058hg38UCSC Ensembl
chr17:39554737..39555310hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242969
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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