A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280897



Internal ID20490115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85911124..85911124hg38UCSC Ensembl
chrX:85166129..85166129hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740996
Supporting Variants
Samples
Known GenesCHM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280897
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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