A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637947



Internal ID7024734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11924452..11941720hg38UCSC Ensembl
chr16:12018309..12035577hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817269
hg1917269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377096, essv15377097, essv15377100, essv15377095, essv15377101, essv15377102, essv15377099, essv15377098
SamplesNA20332, HG03520, HG02976, NA19257, NA19108, NA19256, HG03129, HG00553
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637947
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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