A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291846



Internal ID20501064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120687968..120687968hg38UCSC Ensembl
chrX:119821823..119821823hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291846
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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