A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11390573



Internal ID6956636
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600151
Supporting Variants
SamplesNA21135
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11390573
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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