A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795109



Internal ID21240447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66309095..66309095hg38UCSC Ensembl
chr15:66601433..66601433hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685989
Samples
Known GenesDIS3L
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795109
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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