A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740249



Internal ID18714495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37958916..37959216hg38UCSC Ensembl
Outerchr7:37958851..37959262hg38UCSC Ensembl
Innerchr7:37998518..37998818hg19UCSC Ensembl
Outerchr7:37998453..37998864hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740249
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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