A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11360361



Internal ID1108547
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599755
Supporting Variants
SamplesHG00737
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11360361
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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