A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111399



Internal ID22020633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154410112..154410424hg38UCSC Ensembl
chrX:153638448..153638760hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639485
Samples
Known GenesDNASE1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111399
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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