A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546093



Internal ID18400483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29423224..29423708hg38UCSC Ensembl
Outerchr10:29423163..29423824hg38UCSC Ensembl
Innerchr10:29712153..29712637hg19UCSC Ensembl
Outerchr10:29712092..29712753hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744840
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546093
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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