A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741301



Internal ID18715547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130836..143196751hg38UCSC Ensembl
Outerchr7:143127408..143198705hg38UCSC Ensembl
Innerchr7:142827929..142893844hg19UCSC Ensembl
Outerchr7:142824501..142895798hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3871298
hg1971298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542554
Supporting Variants
Samples
Known GenesPIP, TAS2R39
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741301
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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