A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041919



Internal ID21951247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139144415..139144415hg38UCSC Ensembl
chrX:138226577..138226577hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639571
Samples
Known GenesFGF13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041919
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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