A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744977



Internal ID18719223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44598926..44601288hg38UCSC Ensembl
Outerchr10:44598913..44601476hg38UCSC Ensembl
Innerchr10:45094374..45096736hg19UCSC Ensembl
Outerchr10:45094361..45096924hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382564
hg192564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744977
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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