A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638787



Internal ID7025572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61945694..61961406hg38UCSC Ensembl
Innerchr16:61945694..61961406hg38UCSC Ensembl
Outerchr16:61945599..61961517hg38UCSC Ensembl
chr16:61979598..61995310hg19UCSC Ensembl
Innerchr16:61979598..61995310hg19UCSC Ensembl
Outerchr16:61979503..61995421hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3815713
hg1915713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496301, essv15496302
SamplesHG00692, NA18541
Known GenesCDH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638787
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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