A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744553



Internal ID18718799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4679775..4681925hg38UCSC Ensembl
Outerchr10:4679228..4682103hg38UCSC Ensembl
Innerchr10:4721967..4724117hg19UCSC Ensembl
Outerchr10:4721420..4724295hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382876
hg192876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744553
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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