A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290960



Internal ID20500178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62677453..62677579hg38UCSC Ensembl
chr10:64437213..64437339hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290960
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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