A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416526



Internal ID195747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57754391..58013433hg38UCSC Ensembl
chrX:57780824..58039867hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38259043
hg19259044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740320
Samples
Known GenesZXDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416526
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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