A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762575



Internal ID18390135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47485808..47485860hg38UCSC Ensembl
chr4:47487825..47487877hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563828
Supporting Variants
Samples
Known GenesATP10D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762575
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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