A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678151



Internal ID9597570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89219308..89220179hg38UCSC Ensembl
chr7:88848622..88849493hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5514041, essv6344317, essv6127716, essv5946190, essv5570363, essv5974776, essv5572039, essv5651344, essv5827461, essv5776408, essv6309424
SamplesNA19466, NA19138, NA19471, NA19921, NA19451, NA19236, NA19434, NA19428, NA19311, NA19711, NA19346
Known GenesZNF804B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678151
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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