A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610114



Internal ID6997033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98941246..98943219hg38UCSC Ensembl
Innerchr6:98941246..98943219hg38UCSC Ensembl
Outerchr6:98941058..98943431hg38UCSC Ensembl
chr6:99389122..99391095hg19UCSC Ensembl
Innerchr6:99389122..99391095hg19UCSC Ensembl
Outerchr6:99388934..99391307hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12475488, essv12475483, essv12475489, essv12475487, essv12475484, essv12475479, essv12475486, essv12475485, essv12475482, essv12475480, essv12475492, essv12475491, essv12475481, essv12475490
SamplesNA18621, HG03199, NA20890, HG02756, HG03736, NA18868, NA20889, HG03369, HG03969, NA18593, NA18909, HG03458, HG03432, HG01912
Known GenesFBXL4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610114
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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