A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11030289



Internal ID1838811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65294446..65305067hg38UCSC Ensembl
Innerchr3:65294446..65305067hg38UCSC Ensembl
Outerchr3:65293946..65305567hg38UCSC Ensembl
chr3:65280121..65290742hg19UCSC Ensembl
Innerchr3:65280121..65290742hg19UCSC Ensembl
Outerchr3:65279621..65291242hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810622
hg1910622
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596418
Supporting Variants
SamplesHG01707
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11030289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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