A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191893



Internal ID1193709
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598283
Supporting Variants
SamplesNA19327
Known GenesC3orf33, SLC33A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191893
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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