A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541649



Internal ID18742725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:52735191..52735443hg38UCSC Ensembl
Outerchr7:52735112..52735493hg38UCSC Ensembl
Innerchr7:52802885..52803137hg19UCSC Ensembl
Outerchr7:52802806..52803187hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740396
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541649
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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