A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738925



Internal ID18713171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119016165..119016464hg38UCSC Ensembl
Outerchr1:119016108..119016540hg38UCSC Ensembl
Innerchr1:119558788..119559087hg19UCSC Ensembl
Outerchr1:119558731..119559163hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738925
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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