A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642993



Internal ID21835040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48547459..48547459hg38UCSC Ensembl
chrX:48405847..48405847hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050511
Supporting Variants
Samples
Known GenesTBC1D25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642993
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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