A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451649



Internal ID22509521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23725148..23787394hg38UCSC Ensembl
chrX:23743265..23805511hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3862247
hg1962247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878155
Supporting Variants
Samples
Known GenesACOT9, SAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451649
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00


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