A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11089180



Internal ID5441870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103355125..103368667hg38UCSC Ensembl
Innerchr3:103355175..103368617hg38UCSC Ensembl
Outerchr3:103355017..103368775hg38UCSC Ensembl
chr3:103073969..103087511hg19UCSC Ensembl
Innerchr3:103074019..103087461hg19UCSC Ensembl
Outerchr3:103073861..103087619hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3813543
hg1913543
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597223
Supporting Variants
SamplesNA18961
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11089180
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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