A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542367



Internal ID18396757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169668545..169668704hg38UCSC Ensembl
Outerchr1:169668544..169668712hg38UCSC Ensembl
Innerchr1:169637783..169637942hg19UCSC Ensembl
Outerchr1:169637782..169637950hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741114
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542367
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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