A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594872



Internal ID6635147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36658..319672hg38UCSC Ensembl
chr3:78332..361355hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38283015
hg19283024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10896236, essv10896235, essv10896234
SamplesHG02725, HG01880, HG02238
Known GenesCHL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594872
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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