A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261102



Internal ID20470320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117848076..117848132hg38UCSC Ensembl
chr10:119607587..119607643hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735548
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261102
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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