A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109286



Internal ID22018519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30636481..30636582hg38UCSC Ensembl
chrX:30654598..30654699hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109286
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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