A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639507



Internal ID7026287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87279310..87303441hg38UCSC Ensembl
chr16:87312916..87337047hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3824132
hg1924132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv552e214
Supporting Variantsessv15555123, essv15555122, essv15555124, essv15555125
SamplesHG03817, HG00284, HG00329, HG03894
Known GenesC16orf95, LOC101928682
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639507
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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