A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637849



Internal ID6677949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8837916..8849663hg38UCSC Ensembl
chr16:8931773..8943520hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3811748
hg1911748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15372175, essv15372174
SamplesHG01356, HG01345
Known GenesPMM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637849
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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