A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4158256



Internal ID11440794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17875510..17875616hg38UCSC Ensembl
chr8:17733019..17733125hg19UCSC Ensembl
chr8:17777299..17777405hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38107
hg19107
hg18107
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1091529
Supporting Variants
SamplesHuRef
Known GenesFGL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4158256
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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