A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639521



Internal ID7026301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87659546..87666049hg38UCSC Ensembl
chr16:87693152..87699655hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg386504
hg196504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555198, essv15555196, essv15555197, essv15555195
SamplesNA12751, NA19712, HG03931, HG01786
Known GenesJPH3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639521
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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