A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234337



Internal ID20801378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23209997..23210441hg38UCSC Ensembl
chr10:23498926..23499370hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592867
Supporting Variants
Samples
Known GenesC10orf115
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234337
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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