A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15106772



Internal ID3844570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711855..98730148hg38UCSC Ensembl
chr14:99178192..99196485hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3818294
hg1918294
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635472
Supporting Variants
SamplesHG03478
Known GenesC14orf177
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15106772
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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