A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599732



Internal ID6639995
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv988e214
Supporting Variantsessv11359765
SamplesNA19023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599732
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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