A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271515



Internal ID20480733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63873720..63874591hg38UCSC Ensembl
chr10:65633480..65634351hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739776
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271515
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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