A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599973



Internal ID6640235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25710346..25734271hg38UCSC Ensembl
Innerchr4:25710350..25734267hg38UCSC Ensembl
Outerchr4:25710342..25734275hg38UCSC Ensembl
chr4:25711968..25735893hg19UCSC Ensembl
Innerchr4:25711972..25735889hg19UCSC Ensembl
Outerchr4:25711964..25735897hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3823926
hg1923926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11373397, essv11373399, essv11373402, essv11373398, essv11373393, essv11373400, essv11373396, essv11373394, essv11373395, essv11373401
SamplesNA18988, NA19070, NA19086, NA19084, NA19009, NA19012, NA18974, NA18941, NA18943, NA19060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599973
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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