A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744465



Internal ID18372025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1368124..1368249hg38UCSC Ensembl
Outerchr10:1368115..1368260hg38UCSC Ensembl
Innerchr10:1410319..1410444hg19UCSC Ensembl
Outerchr10:1410310..1410455hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545718
Supporting Variants
Samples
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744465
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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