A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766161



Internal ID18393721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109919668..109920392hg38UCSC Ensembl
Outerchr1:109919634..109920409hg38UCSC Ensembl
Innerchr1:110462290..110463014hg19UCSC Ensembl
Outerchr1:110462256..110463031hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567414
Supporting Variants
Samples
Known GenesCSF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766161
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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