A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231743



Internal ID20798783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102803623..102804388hg38UCSC Ensembl
chr10:104563380..104564145hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575727
Supporting Variants
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231743
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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