A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677901



Internal ID21199758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11682644..11682644hg38UCSC Ensembl
chr10:11724643..11724643hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677901
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.416667


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