A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564912



Internal ID7036012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:71867474..71868207hg38UCSC Ensembl
Outerchr16:71901377..71902110hg19UCSC Ensembl
Outerchr16:70458878..70459611hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg385508
hg195508
hg185508
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001782
Supporting Variants
SamplesHuRef
Known GenesZNF821
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564912
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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