A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4260574



Internal ID11543112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100511751..100512065hg38UCSC Ensembl
chr15:101051956..101052270hg19UCSC Ensembl
chr15:98869479..98869793hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38315
hg19315
hg18315
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1555633
Supporting Variants
SamplesHuRef
Known GenesCERS3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4260574
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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