A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657395



Internal ID9923500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74032091..74081452hg38UCSC Ensembl
chr6:74741807..74791168hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3849362
hg1949362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5900586, essv6235299, essv5506020, essv5891473, essv6071663, essv6336217
SamplesNA20532, NA18988, NA18964, NA18557, NA20801, NA12046
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657395
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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