A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745522



Internal ID18373082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103337780..103338031hg38UCSC Ensembl
Outerchr10:103337718..103338104hg38UCSC Ensembl
Innerchr10:105097537..105097788hg19UCSC Ensembl
Outerchr10:105097475..105097861hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546775
Supporting Variants
Samples
Known GenesPCGF6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745522
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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