A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789802



Internal ID21235140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89998327..89998327hg38UCSC Ensembl
chr10:91758084..91758084hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789802
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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