A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611779



Internal ID6998683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:406539..410166hg38UCSC Ensembl
Innerchr7:406580..410125hg38UCSC Ensembl
Outerchr7:406498..410207hg38UCSC Ensembl
chr7:446505..450132hg19UCSC Ensembl
Innerchr7:446546..450091hg19UCSC Ensembl
Outerchr7:446464..450173hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383628
hg193628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657812
SamplesNA19670
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611779
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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