A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260309



Internal ID20469527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9791968..9792060hg38UCSC Ensembl
chrX:9760008..9760100hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758755
Supporting Variants
Samples
Known GenesSHROOM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260309
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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