A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670059



Internal ID21618366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49966577..49968961hg38UCSC Ensembl
chrX:49731187..49733574hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg382385
hg192388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167449
SamplesNA19238
Known GenesCLCN5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670059
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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