A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744990



Internal ID18372550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46409114..46410244hg38UCSC Ensembl
Outerchr10:46409047..46410513hg38UCSC Ensembl
Innerchr10:47139507..47140637hg19UCSC Ensembl
Outerchr10:47139238..47140704hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381467
hg191467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546243
Supporting Variants
Samples
Known GenesLINC00842
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744990
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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