A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15053932



Internal ID6797824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71179095..71189700hg38UCSC Ensembl
chr14:71645812..71656417hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3810606
hg1910606
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634874
Supporting Variants
SamplesNA20888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15053932
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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