A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740685



Internal ID18714931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:77241225..77241473hg38UCSC Ensembl
Outerchr7:77241163..77241488hg38UCSC Ensembl
Innerchr7:76870542..76870790hg19UCSC Ensembl
Outerchr7:76870480..76870805hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541938
Supporting Variants
Samples
Known GenesCCDC146
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740685
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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