A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101031



Internal ID22010264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111721193..111721318hg38UCSC Ensembl
chrX:110964421..110964546hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646840
Samples
Known GenesALG13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101031
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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