A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692504



Internal ID21214356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118506122..118506122hg38UCSC Ensembl
chr10:120265634..120265634hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692504
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.09375


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