A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541363



Internal ID18395753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26175668..26176131hg38UCSC Ensembl
Outerchr7:26175635..26176160hg38UCSC Ensembl
Innerchr7:26215288..26215751hg19UCSC Ensembl
Outerchr7:26215255..26215780hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740110
Samples
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541363
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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