A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740276



Internal ID18714522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39830442..39830689hg38UCSC Ensembl
Outerchr7:39830416..39830753hg38UCSC Ensembl
Innerchr7:39870041..39870288hg19UCSC Ensembl
Outerchr7:39870015..39870352hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740276
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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