A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794220



Internal ID21239558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55303239..55303239hg38UCSC Ensembl
chr15:55595437..55595437hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794220
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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