A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999314



Internal ID7082149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17875482..17875588hg38UCSC Ensembl
chr8:17732991..17733097hg19UCSC Ensembl
chr8:17777271..17777377hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38107
hg19107
hg18107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3579083
SamplesHuRef
Known GenesFGL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999314
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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