A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074031



Internal ID5430524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96777428..96778236hg38UCSC Ensembl
Innerchr3:96777437..96778228hg38UCSC Ensembl
Outerchr3:96777420..96778245hg38UCSC Ensembl
chr3:96496272..96497080hg19UCSC Ensembl
Innerchr3:96496281..96497072hg19UCSC Ensembl
Outerchr3:96496264..96497089hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597080
Supporting Variants
SamplesNA18956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074031
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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