A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546608



Internal ID18400998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:85620405..85622324hg38UCSC Ensembl
Outerchr10:85620378..85622335hg38UCSC Ensembl
Innerchr10:87380162..87382081hg19UCSC Ensembl
Outerchr10:87380135..87382092hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381958
hg191958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745355
Samples
Known GenesGRID1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546608
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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