A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966431



Internal ID22741366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118452489..118452489hg38UCSC Ensembl
chrX:117586452..117586452hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966431
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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