A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659341



Internal ID9578760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140531574..140532038hg38UCSC Ensembl
chr7:140231374..140231838hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5439418, essv5610219, essv5889675, essv6518120, essv5922419, essv6216640, essv6422302, essv6355727, essv6083979, essv5658888
SamplesNA19701, NA19904, NA19172, NA19437, NA18907, HG01204, NA19375, NA19467, NA19360, NA19900
Known GenesDENND2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659341
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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