A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105652



Internal ID22014885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49834001..49843282hg38UCSC Ensembl
chrX:49598604..49607885hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg389282
hg199282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640477
Samples
Known GenesPAGE4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105652
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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