A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224832



Internal ID20791872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4974858..4993272hg38UCSC Ensembl
chr10:5017050..5035464hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3818415
hg1918415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580415
Supporting Variants
Samples
Known GenesAKR1C1, AKR1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224832
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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