A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795362



Internal ID21240700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69832421..69832421hg38UCSC Ensembl
chr15:70124760..70124760hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13686170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795362
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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