A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11047188



Internal ID3644798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76678715..76759047hg38UCSC Ensembl
chr3:76727866..76808198hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3880333
hg1980333
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596645
Supporting Variants
SamplesHG03240
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11047188
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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