A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764314



Internal ID20540174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135012907..135012907hg38UCSC Ensembl
chrX:134146937..134146937hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764314
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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