A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659894



Internal ID9579313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89324124..89324793hg38UCSC Ensembl
Innerchr7:88953438..88954107hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6564432, essv5551709, essv6192583
SamplesNA19093, NA19239, NA19240
Known GenesZNF804B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659894
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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