A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740885



Internal ID18715131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98599532..98601392hg38UCSC Ensembl
Outerchr7:98599212..98601627hg38UCSC Ensembl
Innerchr7:98228844..98230704hg19UCSC Ensembl
Outerchr7:98228524..98230939hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382416
hg192416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740885
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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