A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11176502



Internal ID6203553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147766673..147806590hg38UCSC Ensembl
Innerchr3:147766673..147806590hg38UCSC Ensembl
Outerchr3:147766173..147807090hg38UCSC Ensembl
chr3:147484460..147524377hg19UCSC Ensembl
Innerchr3:147484460..147524377hg19UCSC Ensembl
Outerchr3:147483960..147524877hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3839918
hg1939918
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598117
Supporting Variants
SamplesNA19731
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11176502
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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