A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274840



Internal ID20484058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152833254..152833254hg38UCSC Ensembl
chrX:152001798..152001798hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758758
Supporting Variants
Samples
Known GenesNSDHL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274840
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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