A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432989



Internal ID211718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6256975..6810945hg38UCSC Ensembl
chrX:6175016..6728986hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38553971
hg19553971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736237
Samples
Known GenesMIR4770, VCX3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432989
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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