A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645347



Internal ID21837394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122435458..122435458hg38UCSC Ensembl
chrX:121569311..121569311hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645347
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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