A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665709



Internal ID9931814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35662937..35664534hg38UCSC Ensembl
chr9:35662934..35664531hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5412098, essv6007409, essv6078521, essv6403575
SamplesNA19648, NA12058, HG00155, NA12830
Known GenesARHGEF39
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665709
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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