A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545899



Internal ID18746975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11896850..11897892hg38UCSC Ensembl
Outerchr1:11896838..11897944hg38UCSC Ensembl
Innerchr1:11956907..11957949hg19UCSC Ensembl
Outerchr1:11956895..11958001hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744646
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545899
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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