A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261389



Internal ID20470607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6160961..6161103hg38UCSC Ensembl
chrX:6079002..6079144hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767125
Supporting Variants
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261389
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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