A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756617



Internal ID20532477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30329643..30330476hg38UCSC Ensembl
chrX:30347760..30348593hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756617
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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