A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585675



Internal ID21777718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101178516..101179745hg38UCSC Ensembl
chr10:102938273..102939502hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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