A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765394



Internal ID18392954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1207388..1207754hg38UCSC Ensembl
Outerchr1:1207320..1207781hg38UCSC Ensembl
Innerchr1:1142768..1143134hg19UCSC Ensembl
Outerchr1:1142700..1143161hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765394
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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