A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599819



Internal ID6986864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19478584..19507308hg38UCSC Ensembl
Innerchr4:19479084..19506808hg38UCSC Ensembl
Outerchr4:19477584..19508308hg38UCSC Ensembl
chr4:19480207..19508931hg19UCSC Ensembl
Innerchr4:19480707..19508431hg19UCSC Ensembl
Outerchr4:19479207..19509931hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3828725
hg1928725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11365846
SamplesHG00654
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599819
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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