A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801286



Internal ID21246624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21461252..21461315hg38UCSC Ensembl
chr1:21787745..21787808hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681603
Samples
Known GenesNBPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801286
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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