A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599755



Internal ID6986800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16369971..16405082hg38UCSC Ensembl
Innerchr4:16370121..16404932hg38UCSC Ensembl
Outerchr4:16369821..16405232hg38UCSC Ensembl
chr4:16371594..16406705hg19UCSC Ensembl
Innerchr4:16371744..16406555hg19UCSC Ensembl
Outerchr4:16371444..16406855hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3835112
hg1935112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv989e214
Supporting Variantsessv11360361, essv11360363, essv11360360, essv11360362, essv11360364, essv11360365
SamplesHG00737, HG00610, NA19917, HG02508, NA19428, HG01431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599755
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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