A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581252



Internal ID21773295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110295559..110295559hg38UCSC Ensembl
chr10:112055317..112055317hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081475
Supporting Variants
Samples
Known GenesSMNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581252
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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