A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15108806



Internal ID5110622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101288266..101429571hg38UCSC Ensembl
chr14:101754603..101895908hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38141306
hg19141306
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635526
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15108806
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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