A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541304



Internal ID18742380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20231630..20237877hg38UCSC Ensembl
Outerchr7:20230878..20238921hg38UCSC Ensembl
Innerchr7:20271253..20277500hg19UCSC Ensembl
Outerchr7:20270501..20278544hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg388044
hg198044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740051
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541304
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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