A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637933



Internal ID6678032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11697174..11706685hg38UCSC Ensembl
chr16:11791030..11800541hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg389512
hg199512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377010
SamplesHG04029
Known GenesTXNDC11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637933
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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