A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583069



Internal ID21775112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45071853..45072537hg38UCSC Ensembl
chr10:45567301..45567985hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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