A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788331



Internal ID21233669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114306316..114306316hg38UCSC Ensembl
chr10:116066075..116066075hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689636, nssv13683058
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788331
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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