A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645129



Internal ID21837176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16714536..16714536hg38UCSC Ensembl
chrX:16732659..16732659hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645129
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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