A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231699



Internal ID20798739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116957344..116957888hg38UCSC Ensembl
chr10:118716855..118717399hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591319
Supporting Variants
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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