A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11069210



Internal ID5895066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89881807..89887937hg38UCSC Ensembl
Innerchr3:89881857..89887887hg38UCSC Ensembl
Outerchr3:89881757..89887987hg38UCSC Ensembl
chr3:89930957..89937087hg19UCSC Ensembl
Innerchr3:89931007..89937037hg19UCSC Ensembl
Outerchr3:89930907..89937137hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg386131
hg196131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596979
Supporting Variants
SamplesNA19315
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11069210
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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