A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731650



Internal ID20507570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73594783..73594783hg38UCSC Ensembl
chrX:72814619..72814619hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277727
Samples
Known GenesCHIC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731650
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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