A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634692



Internal ID7021495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61838191..61862389hg38UCSC Ensembl
chr14:62304909..62329107hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3824199
hg1924199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15036712
SamplesHG03084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634692
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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