A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794976



Internal ID21240314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60365043..60365043hg38UCSC Ensembl
chr15:60657242..60657242hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694574
Samples
Known GenesANXA2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794976
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer