A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2810633



Internal ID21255971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178302316..178302316hg38UCSC Ensembl
chr5:177729317..177729317hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705004
Samples
Known GenesCOL23A1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2810633
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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