A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903594



Internal ID905410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4084346..4217948hg38UCSC Ensembl
chr3:4126030..4259632hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38133603
hg19133603
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595083
Supporting Variants
SamplesNA19385
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903594
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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