A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752717



Internal ID20528577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103892093..103897752hg38UCSC Ensembl
chrX:103147014..103152673hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280724
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752717
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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