A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957249



Internal ID22732377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3942658..3942658hg38UCSC Ensembl
chrX:3860699..3860699hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957249
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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