A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562371



Internal ID18763447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:56365531..56369282hg38UCSC Ensembl
Outerchr1:56365402..56369411hg38UCSC Ensembl
Innerchr1:56831203..56834954hg19UCSC Ensembl
Outerchr1:56831074..56835083hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg384010
hg194010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761118
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562371
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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