A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997568



Internal ID6733510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88000199..88000996hg38UCSC Ensembl
chr16:88033805..88034602hg19UCSC Ensembl
chr16:86591306..86592103hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38798
hg19798
hg18798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3577934
SamplesHuRef
Known GenesBANP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997568
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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