A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750902



Internal ID20526762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21635195..21635360hg38UCSC Ensembl
chrX:21653313..21653478hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275182
Samples
Known GenesCNKSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750902
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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