A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595085



Internal ID6982404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4099243..4142900hg38UCSC Ensembl
Innerchr3:4099743..4142400hg38UCSC Ensembl
Outerchr3:4098243..4143900hg38UCSC Ensembl
chr3:4140927..4184584hg19UCSC Ensembl
Innerchr3:4141427..4184084hg19UCSC Ensembl
Outerchr3:4139927..4185584hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3843658
hg1943658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv865e214
Supporting Variantsessv10903623, essv10903618, essv10903630, essv10903627, essv10903621, essv10903629, essv10903624, essv10903622, essv10903619, essv10903625, essv10903620, essv10903631, essv10903626, essv10903628
SamplesHG00766, HG02600, HG03518, NA19098, HG01046, HG03814, NA18557, NA20903, HG04054, NA20542, HG03934, HG00728, NA20502, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595085
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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