A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803163



Internal ID21248501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51961654..51961654hg38UCSC Ensembl
chr20:50578193..50578193hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803163
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