A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992101



Internal ID7077775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163611651..163611718hg38UCSC Ensembl
chr6:164032683..164032750hg19UCSC Ensembl
chr6:163952673..163952740hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3578858
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992101
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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