A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545322



Internal ID18746398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203373210..203373260hg38UCSC Ensembl
Outerchr1:203373207..203373266hg38UCSC Ensembl
Innerchr1:203342338..203342388hg19UCSC Ensembl
Outerchr1:203342335..203342394hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744069
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545322
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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