A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637936



Internal ID6678035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11731064..11736120hg38UCSC Ensembl
chr16:11824920..11829976hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg385057
hg195057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377014, essv15377013
SamplesNA18640, NA18945
Known GenesTXNDC11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637936
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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