A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286807



Internal ID20496025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21731428..21731428hg38UCSC Ensembl
chrX:21749546..21749546hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733443
Supporting Variants
Samples
Known GenesSMPX
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286807
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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