A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3576826



Internal ID6701522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10462410..10462657hg38UCSC Ensembl
chr18:10462407..10462654hg19UCSC Ensembl
chr18:10452407..10452654hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38248
hg19248
hg18248
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988512
Supporting Variants
SamplesHuRef
Known GenesAPCDD1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3576826
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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