A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542527



Internal ID18743603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140908813..140908998hg38UCSC Ensembl
Outerchr7:140908765..140909017hg38UCSC Ensembl
Innerchr7:140608613..140608798hg19UCSC Ensembl
Outerchr7:140608565..140608817hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741274
Samples
Known GenesBRAF
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542527
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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