A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11359765



Internal ID1361581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14685631..14802339hg38UCSC Ensembl
chr4:14687255..14803963hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38116709
hg19116709
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599732
Supporting Variants
SamplesNA19023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11359765
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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