A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439361



Internal ID22497231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16709157..16709579hg38UCSC Ensembl
chrX:16727280..16727702hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877456
Supporting Variants
Samples
Known GenesCTPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439361
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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