A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796007



Internal ID21241345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3656331..3656331hg38UCSC Ensembl
chr16:3706332..3706332hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690714
Samples
Known GenesDNASE1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796007
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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