A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226580



Internal ID20793620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97251842..97251966hg38UCSC Ensembl
chr10:99011599..99011723hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590599
Supporting Variants
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226580
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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