A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296857



Internal ID20506075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102184275..102184275hg38UCSC Ensembl
chrX:101439248..101439248hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg381523
hg191523
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744644
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296857
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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