A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585143



Internal ID20958214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114052867..114055359hg38UCSC Ensembl
chr10:115812626..115815118hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382493
hg192493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585143
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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