A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10968964



Internal ID1942054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30227012..30305649hg38UCSC Ensembl
chr3:30268503..30347140hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3878638
hg1978638
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595734
Supporting Variants
SamplesHG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10968964
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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