A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745125



Internal ID20521130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24078507..24078507hg38UCSC Ensembl
chrX:24096624..24096624hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272556
Samples
Known GenesEIF2S3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745125
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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