A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638564



Internal ID7025349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47550128..47632867hg38UCSC Ensembl
chr16:47584039..47666778hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3882740
hg1982740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15472442
SamplesNA21137
Known GenesPHKB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638564
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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