A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597310



Internal ID6637580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107540473..107549147hg38UCSC Ensembl
Innerchr3:107540477..107549143hg38UCSC Ensembl
Outerchr3:107540469..107549151hg38UCSC Ensembl
chr3:107259320..107267994hg19UCSC Ensembl
Innerchr3:107259324..107267990hg19UCSC Ensembl
Outerchr3:107259316..107267998hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388675
hg198675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11096579
SamplesNA19152
Known GenesBBX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597310
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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