A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880317



Internal ID22655287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17484630..17484698hg38UCSC Ensembl
chrX:17502753..17502821hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440585
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880317
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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