A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954799



Internal ID22730027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134955675..134955675hg38UCSC Ensembl
chrX:134089705..134089705hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954799
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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