A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788859



Internal ID21234197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21057597..21057597hg38UCSC Ensembl
chr10:21346526..21346526hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699906
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788859
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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