A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875126



Internal ID22650081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154827466..154829279hg38UCSC Ensembl
chrX:154055741..154057554hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440229
Samples
Known GenesSMIM9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875126
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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