A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541495



Internal ID18395885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37310977..37311217hg38UCSC Ensembl
Outerchr7:37310920..37311222hg38UCSC Ensembl
Innerchr7:37350581..37350821hg19UCSC Ensembl
Outerchr7:37350524..37350826hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740242
Samples
Known GenesELMO1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541495
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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