A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610429



Internal ID6650655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114283545..114291432hg38UCSC Ensembl
Innerchr6:114283549..114291429hg38UCSC Ensembl
Outerchr6:114283542..114291436hg38UCSC Ensembl
chr6:114604709..114612596hg19UCSC Ensembl
Innerchr6:114604713..114612593hg19UCSC Ensembl
Outerchr6:114604706..114612600hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg387888
hg197888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12508959, essv12508960, essv12508954, essv12508956, essv12508957, essv12508953, essv12508955, essv12508962, essv12508958, essv12508961, essv12508963
SamplesHG03295, HG03046, HG03548, NA20356, HG03225, HG03085, HG03073, NA20318, HG02481, NA20317, HG03240
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610429
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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