A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765361



Internal ID18739607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101822810..101824013hg38UCSC Ensembl
Outerchr1:101822786..101824042hg38UCSC Ensembl
Innerchr1:102288366..102289569hg19UCSC Ensembl
Outerchr1:102288342..102289598hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566614
Supporting Variants
Samples
Known GenesOLFM3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765361
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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