A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107956



Internal ID22017191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123023085..123023227hg38UCSC Ensembl
chrX:122156938..122157080hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107956
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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