A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547199



Internal ID321075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20775656..20823762hg38UCSC Ensembl
chrX:20793774..20841880hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3848107
hg1948107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547199
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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