A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100926



Internal ID22010159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125929139..125936027hg38UCSC Ensembl
chrX:125063121..125070009hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg386889
hg196889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100926
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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