A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044873



Internal ID21954151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115191466..115191466hg38UCSC Ensembl
chrX:114426029..114426029hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640398
Samples
Known GenesLRCH2, RBMXL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044873
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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