A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243237



Internal ID20810277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7796098..7796940hg38UCSC Ensembl
chr17:7699416..7700258hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595064
Supporting Variants
Samples
Known GenesDNAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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