A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549071



Internal ID322770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28572586..28573272hg38UCSC Ensembl
chrX:28590703..28591389hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549071
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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