A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741375



Internal ID18715621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149156633..149157275hg38UCSC Ensembl
Outerchr7:149156601..149157291hg38UCSC Ensembl
Innerchr7:148853725..148854367hg19UCSC Ensembl
Outerchr7:148853693..148854383hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542628
Supporting Variants
Samples
Known GenesZNF398
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741375
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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