A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586794



Internal ID20959865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97239745..97240486hg38UCSC Ensembl
chr10:98999502..99000243hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217705
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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