A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740894



Internal ID18715140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99373473..99373648hg38UCSC Ensembl
chr7:98971096..98971271hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740894
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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