A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761884



Internal ID20537744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127503322..127503322hg38UCSC Ensembl
chrX:126637303..126637303hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38974
hg19974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761884
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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