A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5776408



Internal ID8753811
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 Flag1
Merged StatusS
Merged Variantsesv2678151
Supporting Variants
SamplesNA19346
Known GenesZNF804B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5776408
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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