A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800882



Internal ID21246220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154755504..154755504hg38UCSC Ensembl
chr1:154727980..154727980hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682003
Samples
Known GenesKCNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800882
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