A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543358



Internal ID18744434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36213032..36219213hg38UCSC Ensembl
Outerchr8:36212483..36220161hg38UCSC Ensembl
Innerchr8:36070550..36076731hg19UCSC Ensembl
Outerchr8:36070001..36077679hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg387679
hg197679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742105
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543358
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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