A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537390



Internal ID312677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130579211..130579211hg38UCSC Ensembl
chrX:129713185..129713185hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537390
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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