A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546492



Internal ID18400882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72064902..72065202hg38UCSC Ensembl
Outerchr10:72064898..72065206hg38UCSC Ensembl
Innerchr10:73824660..73824960hg19UCSC Ensembl
Outerchr10:73824656..73824964hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745239
Samples
Known GenesSPOCK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546492
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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