A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588954



Internal ID21780997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118423950..118423950hg38UCSC Ensembl
chr10:120183462..120183462hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384091
hg194091
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588954
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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