A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599751



Internal ID6986796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16292366..16302027hg38UCSC Ensembl
Innerchr4:16292400..16301994hg38UCSC Ensembl
Outerchr4:16292333..16302061hg38UCSC Ensembl
chr4:16293989..16303650hg19UCSC Ensembl
Innerchr4:16294023..16303617hg19UCSC Ensembl
Outerchr4:16293956..16303684hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389662
hg199662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11360353
SamplesHG02111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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