A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3939316



Internal ID11822556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22708974..22709390hg38UCSC Ensembl
chr8:22566487..22566903hg19UCSC Ensembl
chr8:22622432..22622848hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38417
hg19417
hg18417
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1312882
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3939316
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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