A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806573



Internal ID21251911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74176276..74176276hg38UCSC Ensembl
chr2:74403403..74403403hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690136
Samples
Known GenesMOB1A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806573
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