A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659913



Internal ID5190198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157237968..157303891hg38UCSC Ensembl
chr4:158159120..158225043hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3865924
hg1965924
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602806
Supporting Variants
SamplesNA18610
Known GenesGRIA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659913
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