A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635591



Internal ID6675704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103355152..103434788hg38UCSC Ensembl
Innerchr14:103355302..103434638hg38UCSC Ensembl
Outerchr14:103355002..103434938hg38UCSC Ensembl
chr14:103821489..103901125hg19UCSC Ensembl
Innerchr14:103821639..103900975hg19UCSC Ensembl
Outerchr14:103821339..103901275hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3879637
hg1979637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv422e214
Supporting Variantsessv15114325, essv15114324, essv15114326
SamplesNA12341, NA06984, HG00598
Known GenesMARK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635591
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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