A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1556167



Internal ID12719288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90684600..90685447hg38UCSC Ensembl
chr8:91696828..91697675hg19UCSC Ensembl
chr8:91766004..91766851hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38848
hg19848
hg18848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4351616
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1556167
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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