A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751453



Internal ID18725699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77444962..77445040hg38UCSC Ensembl
chr15:77737304..77737382hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552706
Supporting Variants
Samples
Known GenesHMG20A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751453
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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