A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645217



Internal ID21837264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146382754..146382754hg38UCSC Ensembl
chrX:145464272..145464272hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645217
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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