A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235706



Internal ID20802746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44495102..44495281hg38UCSC Ensembl
chr10:44990550..44990729hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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