A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744975



Internal ID18372535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44313199..44315113hg38UCSC Ensembl
Outerchr10:44313057..44315138hg38UCSC Ensembl
Innerchr10:44808647..44810561hg19UCSC Ensembl
Outerchr10:44808505..44810586hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744975
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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