A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639353



Internal ID7026135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82134351..82201089hg38UCSC Ensembl
chr16:82167956..82234694hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3866739
hg1966739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15542308
SamplesHG03607
Known GenesMPHOSPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639353
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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