A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261969



Internal ID20471187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112709915..112709915hg38UCSC Ensembl
chrX:111953143..111953143hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261969
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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