A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549148



Internal ID20922316
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 StatusM
Merged Variants
Supporting Variantsnssv18248190
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)nsv6549148
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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