A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662732



Internal ID9928837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196199732..196201511hg38UCSC Ensembl
chr3:195926603..195928382hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5946745, essv6157890, essv5857082, essv5737250, essv6195841, essv5819840, essv6280116, essv5506313, essv5631538, essv5868853, essv5934758
SamplesHG01098, NA18861, NA19377, NA18489, NA19651, NA19462, NA20799, NA19380, NA19428, NA20348, NA19248
Known GenesZDHHC19
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662732
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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