A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000857



Internal ID7065986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:57287822..57295835hg38UCSC Ensembl
Outerchr16:57321734..57329747hg19UCSC Ensembl
Outerchr16:55879235..55887248hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg388014
hg198014
hg188014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564306
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000857
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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