A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235442



Internal ID20802482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21671584..21672344hg38UCSC Ensembl
chr10:21960513..21961273hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585025
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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