A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444081



Internal ID22501951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151478982..151496057hg38UCSC Ensembl
chrX:150647454..150664529hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3817076
hg1917076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444081
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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