A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4307602



Internal ID11590140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325076..89325274hg38UCSC Ensembl
chr15:89868307..89868505hg19UCSC Ensembl
chr15:87669311..87669509hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38199
hg19199
hg18199
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1642918
Supporting Variants
SamplesHuRef
Known GenesPOLG
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4307602
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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