A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637980



Internal ID7024766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13390462..13395160hg38UCSC Ensembl
chr16:13484319..13489017hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg384699
hg194699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15378542, essv15378543, essv15378545, essv15378544
SamplesNA18561, HG01354, HG00273, HG00319
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637980
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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