A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736875



Internal ID20512828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27514199..27514199hg38UCSC Ensembl
chrX:27532316..27532316hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736875
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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