A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597276



Internal ID21789319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23134573..23134573hg38UCSC Ensembl
chr10:23423502..23423502hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597276
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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