A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3579083



Internal ID7050465
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 StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999314
Supporting Variants
SamplesHuRef
Known GenesFGL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3579083
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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