A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541387



Internal ID18395777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28557028..28557224hg38UCSC Ensembl
Outerchr7:28556997..28557258hg38UCSC Ensembl
Innerchr7:28596646..28596842hg19UCSC Ensembl
Outerchr7:28596615..28596876hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740134
Samples
Known GenesCREB5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541387
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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