A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595086



Internal ID6635361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4100349..4167284hg38UCSC Ensembl
Innerchr3:4100365..4167269hg38UCSC Ensembl
Outerchr3:4100334..4167300hg38UCSC Ensembl
chr3:4142033..4208968hg19UCSC Ensembl
Innerchr3:4142049..4208953hg19UCSC Ensembl
Outerchr3:4142018..4208984hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3866936
hg1966936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10903634, essv10903643, essv10903638, essv10903632, essv10903635, essv10903633, essv10903636, essv10903642, essv10903641, essv10903640, essv10903637, essv10903639
SamplesHG00766, HG03518, NA19098, HG01046, HG03814, NA18557, NA20903, HG04054, NA20542, HG03934, HG00728, NA20502
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595086
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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