A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597362



Internal ID6984590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109913438..109916618hg38UCSC Ensembl
Innerchr3:109913456..109916600hg38UCSC Ensembl
Outerchr3:109913420..109916636hg38UCSC Ensembl
chr3:109632285..109635465hg19UCSC Ensembl
Innerchr3:109632303..109635447hg19UCSC Ensembl
Outerchr3:109632267..109635483hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383181
hg193181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11098311, essv11098312, essv11098310, essv11098309
SamplesHG03300, HG02976, HG03202, NA18517
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597362
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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