A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600151



Internal ID6987195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33359907..33383350hg38UCSC Ensembl
Innerchr4:33359957..33383300hg38UCSC Ensembl
Outerchr4:33359857..33383400hg38UCSC Ensembl
chr4:33361529..33384972hg19UCSC Ensembl
Innerchr4:33361579..33384922hg19UCSC Ensembl
Outerchr4:33361479..33385022hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3823444
hg1923444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11390573, essv11390572, essv11390571
SamplesNA21135, NA19041, NA19445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600151
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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