A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235441



Internal ID20802481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17886843..17887369hg38UCSC Ensembl
chr10:18175772..18176298hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584374
Supporting Variants
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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