A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608391



Internal ID6995321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25893685..25905376hg38UCSC Ensembl
Innerchr6:25893694..25905368hg38UCSC Ensembl
Outerchr6:25893677..25905385hg38UCSC Ensembl
chr6:25893913..25905604hg19UCSC Ensembl
Innerchr6:25893922..25905596hg19UCSC Ensembl
Outerchr6:25893905..25905613hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3811692
hg1911692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12232483, essv12232482, essv12232480, essv12232481
SamplesNA19066, NA18962, NA19076, NA18951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608391
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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