A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871481



Internal ID22646419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22445774..22447312hg38UCSC Ensembl
chrX:22463891..22465429hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381539
hg191539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466318
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871481
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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