A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795286



Internal ID21240624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71199880..71199880hg38UCSC Ensembl
chr15:71492219..71492219hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678093
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795286
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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