A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566807



Internal ID18767883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150062188..150062529hg38UCSC Ensembl
Outerchr5:150062156..150062611hg38UCSC Ensembl
Innerchr5:149441751..149442092hg19UCSC Ensembl
Outerchr5:149441719..149442174hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765554
Samples
Known GenesCSF1R
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566807
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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