A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15062218



Internal ID1976968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74661789..74676425hg38UCSC Ensembl
chr14:75128492..75143128hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3814637
hg1914637
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634950
Supporting Variants
SamplesHG01842
Known GenesAREL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15062218
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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