A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637586



Internal ID6677689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:798995..892120hg38UCSC Ensembl
chr16:848995..942120hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3893126
hg1993126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355401
SamplesHG00759
Known GenesGNG13, LMF1, PRR25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637586
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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