A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11314826



Internal ID1316642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:268827..291892hg38UCSC Ensembl
chr4:262616..285681hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3823066
hg1923066
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599366
Supporting Variants
SamplesHG02304
Known GenesZNF732
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11314826
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer