A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744899



Internal ID18372459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35191406..35192709hg38UCSC Ensembl
Outerchr10:35191349..35192791hg38UCSC Ensembl
Innerchr10:35480334..35481637hg19UCSC Ensembl
Outerchr10:35480277..35481719hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546152
Supporting Variants
Samples
Known GenesCREM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744899
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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