A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758630



Internal ID18732876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:104929167..104933361hg38UCSC Ensembl
Outerchr2:104928543..104933696hg38UCSC Ensembl
Innerchr2:105545625..105549819hg19UCSC Ensembl
Outerchr2:105545001..105550154hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg385154
hg195154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758630
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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