A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281255



Internal ID20490473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40211105..40211105hg38UCSC Ensembl
chrX:40070358..40070358hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281255
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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