A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248190



Internal ID20815230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197405080..199905342hg38UCSC Ensembl
chr1:197374210..199874470hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg382500263
hg192500261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549148
Supporting Variants
Samples
Known GenesATP6V1G3, C1orf53, CRB1, DENND1B, LHX9, MIR181A1, MIR181A1HG, MIR181B1, NEK7, PTPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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