A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15089560



Internal ID4723360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85316151..85411769hg38UCSC Ensembl
chr14:85782495..85878113hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3895619
hg1995619
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635187
Supporting Variants
SamplesNA06984
Known GenesLINC00911
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15089560
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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