A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275113



Internal ID20484331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15915717..15921770hg38UCSC Ensembl
chr10:15957716..15963769hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386054
hg196054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749251
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275113
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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