A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598563



Internal ID6985699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167395421..167399078hg38UCSC Ensembl
Innerchr3:167395421..167399078hg38UCSC Ensembl
Outerchr3:167395078..167399412hg38UCSC Ensembl
chr3:167113209..167116866hg19UCSC Ensembl
Innerchr3:167113209..167116866hg19UCSC Ensembl
Outerchr3:167112866..167117200hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg383658
hg193658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11218900, essv11218896, essv11218898, essv11218901, essv11218905, essv11218897, essv11218899, essv11218902, essv11218904, essv11218903
SamplesHG03490, NA12283, HG03762, HG03746, HG00260, HG03900, HG03634, HG03694, NA21117, NA20520
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598563
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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