A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788202



Internal ID21233540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111242690..111242756hg38UCSC Ensembl
chr10:113002448..113002514hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788202
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