A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761469



Internal ID20537329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120694763..120694827hg38UCSC Ensembl
chrX:119828618..119828682hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761469
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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