A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740573



Internal ID18714819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67767810..67768621hg38UCSC Ensembl
Outerchr7:67767756..67768660hg38UCSC Ensembl
Innerchr7:67232797..67233608hg19UCSC Ensembl
Outerchr7:67232743..67233647hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740573
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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