A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101253



Internal ID22010486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80591346..80591476hg38UCSC Ensembl
chrX:79846845..79846975hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101253
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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