A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664697



Internal ID9930802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186638762..186639041hg38UCSC Ensembl
chr4:187559916..187560195hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6205849, essv5602901, essv5727359
SamplesNA19394, NA19396, NA19372
Known GenesFAT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664697
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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