A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467599



Internal ID22525490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39869755..39869874hg38UCSC Ensembl
chrX:39729009..39729128hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467599
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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