A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808538



Internal ID21253876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791596..15791819hg38UCSC Ensembl
chr4:15793219..15793442hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695119
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808538
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