A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219018



Internal ID20786058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15059239..15059843hg38UCSC Ensembl
chr10:15101238..15101842hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586662
Supporting Variants
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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