A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9759839



Internal ID18387399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1029637..1029969hg38UCSC Ensembl
Outerchr1:1029600..1029999hg38UCSC Ensembl
Innerchr1:965017..965349hg19UCSC Ensembl
Outerchr1:964980..965379hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561092
Supporting Variants
Samples
Known GenesAGRN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9759839
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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