A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544937



Internal ID20918175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172815509..173473302hg38UCSC Ensembl
chr1:172784649..173442441hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38657794
hg19657793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248104
Samples
Known GenesLOC100506023, TNFSF18, TNFSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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