A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218765



Internal ID20785805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5851686..5852882hg38UCSC Ensembl
chr10:5893649..5894845hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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