A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750958



Internal ID18725204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8556277..8556365hg38UCSC Ensembl
chr2:8696407..8696495hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750958
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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