A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598283



Internal ID6638548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155759067..155869415hg38UCSC Ensembl
chr3:155476856..155587204hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38110349
hg19110349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191894, essv11191891, essv11191893, essv11191892
SamplesHG02325, NA19327, HG01551, NA21088
Known GenesC3orf33, SLC33A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598283
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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