A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732924



Internal ID20508850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26397668..26397668hg38UCSC Ensembl
chrX:26415785..26415785hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732924
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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