A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795292



Internal ID21240630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599766..78599766hg38UCSC Ensembl
chr15:78892108..78892108hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687626, nssv13677523
Samples
Known GenesCHRNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795292
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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