A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811426



Internal ID21256764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:72209026..72209026hg38UCSC Ensembl
chr4:73074743..73074743hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811426
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