A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291520



Internal ID20500738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87205276..87205276hg38UCSC Ensembl
chrX:86460279..86460279hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291520
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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