A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763310



Internal ID20539170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10244286..10248203hg38UCSC Ensembl
chrX:10212326..10216243hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg383918
hg193918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763310
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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