A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903499



Internal ID905315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3907300..4080268hg38UCSC Ensembl
chr3:3948984..4121952hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38172969
hg19172969
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595072
Supporting Variants
SamplesNA20798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903499
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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