A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110713



Internal ID22019946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72179271..72179401hg38UCSC Ensembl
chrX:71399121..71399251hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110713
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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