A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599638



Internal ID6986683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11015047..11061860hg38UCSC Ensembl
Innerchr4:11015047..11061860hg38UCSC Ensembl
Outerchr4:11014547..11062360hg38UCSC Ensembl
chr4:11016671..11063484hg19UCSC Ensembl
Innerchr4:11016671..11063484hg19UCSC Ensembl
Outerchr4:11016171..11063984hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3846814
hg1946814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11356829
SamplesNA19001
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599638
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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