A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741938



Internal ID20517917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101515265..101515265hg38UCSC Ensembl
chrX:100770252..100770252hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291973
Samples
Known GenesARMCX4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741938
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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