A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639508



Internal ID7026288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87282637..87301052hg38UCSC Ensembl
Innerchr16:87282637..87301052hg38UCSC Ensembl
Outerchr16:87282137..87301552hg38UCSC Ensembl
chr16:87316243..87334658hg19UCSC Ensembl
Innerchr16:87316243..87334658hg19UCSC Ensembl
Outerchr16:87315743..87335158hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3818416
hg1918416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv552e214
Supporting Variantsessv15555126, essv15555127
SamplesHG03817, HG03894
Known GenesLOC101928682
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639508
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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