A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101255



Internal ID22010488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150777634..150780362hg38UCSC Ensembl
chrX:149946107..149948835hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649125
Samples
Known GenesCD99L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101255
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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