A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564837



Internal ID18419227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81707816..81711683hg38UCSC Ensembl
Outerchr1:81707302..81712156hg38UCSC Ensembl
Innerchr1:82173501..82177368hg19UCSC Ensembl
Outerchr1:82172987..82177841hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg384855
hg194855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763584
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564837
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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