A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1076593



Internal ID11893032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89579828..89580256hg38UCSC Ensembl
chr16:89646236..89646664hg19UCSC Ensembl
chr16:88173737..88174165hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38429
hg19429
hg18429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4077513
SamplesHuRef
Known GenesCPNE7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1076593
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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