A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738536



Internal ID18366079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6379317..6385440hg38UCSC Ensembl
Outerchr1:6377830..6385940hg38UCSC Ensembl
Innerchr1:6439377..6445500hg19UCSC Ensembl
Outerchr1:6437890..6446000hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg388111
hg198111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3539789
Supporting Variants
Samples
Known GenesACOT7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738536
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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