A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586791



Internal ID6711487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:100107536..100108031hg38UCSC Ensembl
Innerchr1:100573092..100573587hg19UCSC Ensembl
Innerchr1:100345680..100346175hg18UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38496
hg19496
hg18496
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008570
Supporting Variants
SamplesHuRef
Known GenesSASS6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586791
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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