A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578014



Internal ID20951085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102747164..102747834hg38UCSC Ensembl
chr10:104506921..104507591hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236165
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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