A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947952



Internal ID22723444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109818590..109818590hg38UCSC Ensembl
chrX:109061819..109061819hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947952
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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