A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953494



Internal ID22728773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122435458..122435458hg38UCSC Ensembl
chrX:121569311..121569311hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953494
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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