A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639070



Internal ID7025854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74553492..74567912hg38UCSC Ensembl
Innerchr16:74553992..74567412hg38UCSC Ensembl
Outerchr16:74552492..74568912hg38UCSC Ensembl
chr16:74587390..74601810hg19UCSC Ensembl
Innerchr16:74587890..74601310hg19UCSC Ensembl
Outerchr16:74586390..74602810hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3814421
hg1914421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15518745
SamplesHG03856
Known GenesGLG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639070
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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