A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734557



Internal ID20510494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42285660..42285660hg38UCSC Ensembl
chrX:42144912..42144912hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734557
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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