A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104358



Internal ID22013592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47746249..47750097hg38UCSC Ensembl
chrX:47605648..47609496hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383849
hg193849
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104358
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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