A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1056304



Internal ID11872743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88712925..88712925hg38UCSC Ensembl
chr16:88779333..88779333hg19UCSC Ensembl
chr16:87306834..87306834hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3884
hg1984
hg1884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3926751
SamplesHuRef
Known GenesCTU2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1056304
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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