A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244566



Internal ID20811606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73078239..73078431hg38UCSC Ensembl
chr17:71074378..71074570hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576897
Supporting Variants
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244566
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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