A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600288



Internal ID6987332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39663619..39675541hg38UCSC Ensembl
Innerchr4:39663619..39675541hg38UCSC Ensembl
Outerchr4:39663119..39676041hg38UCSC Ensembl
chr4:39665239..39677161hg19UCSC Ensembl
Innerchr4:39665239..39677161hg19UCSC Ensembl
Outerchr4:39664739..39677661hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3811923
hg1911923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11401397, essv11401396
SamplesHG03578, HG01363
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600288
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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