A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795646



Internal ID21240984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8737990..8737990hg38UCSC Ensembl
chr16:8831847..8831847hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678166
Samples
Known GenesABAT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795646
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