A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789647



Internal ID21234985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32031878..32031878hg38UCSC Ensembl
chr10:32320806..32320806hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695090, nssv13689899
Samples
Known GenesKIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789647
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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