A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416201



Internal ID195438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41380246..41510400hg38UCSC Ensembl
chrX:41239499..41369653hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38130155
hg19130155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736572
Samples
Known GenesNYX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416201
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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