A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749933



Internal ID20525968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85135740..85135740hg38UCSC Ensembl
chrX:84390746..84390746hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749933
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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