A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542762



Internal ID18743838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156507748..156521126hg38UCSC Ensembl
Outerchr7:156504635..156522306hg38UCSC Ensembl
Innerchr7:156300442..156313820hg19UCSC Ensembl
Outerchr7:156297329..156315000hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3817672
hg1917672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741509
Samples
Known GenesLINC01006
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542762
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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