A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668984



Internal ID9588403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149079840..149113788hg38UCSC Ensembl
Outerchr7:149079803..149113838hg38UCSC Ensembl
Innerchr7:148776932..148810880hg19UCSC Ensembl
Outerchr7:148776895..148810930hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3834036
hg1934036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6262896
SamplesHG00280
Known GenesZNF425, ZNF786
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668984
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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