A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880174



Internal ID22655144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118282459..118282577hg38UCSC Ensembl
chrX:117416422..117416540hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880174
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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