A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689636



Internal ID21211490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114306316..114306316hg38UCSC Ensembl
chr10:116066075..116066075hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788331
Supporting Variants
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689636
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.916667


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