A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585948



Internal ID21777991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98274630..98277363hg38UCSC Ensembl
chr10:100034387..100037120hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015752
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585948
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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