A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872463



Internal ID22647403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118339351..118340030hg38UCSC Ensembl
chrX:117473314..117473993hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872463
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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