A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963233



Internal ID22738168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22232596..22232596hg38UCSC Ensembl
chrX:22250713..22250713hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456332
Samples
Known GenesPHEX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963233
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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