A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766188



Internal ID20542048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136023165..136023217hg38UCSC Ensembl
chrX:135105324..135105376hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260462
Samples
Known GenesSLC9A6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766188
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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