A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541549



Internal ID18742625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42323902..42353740hg38UCSC Ensembl
Outerchr7:42323402..42354401hg38UCSC Ensembl
Innerchr7:42363501..42393339hg19UCSC Ensembl
Outerchr7:42363001..42394000hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3831000
hg1931000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740296
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541549
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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