A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595082



Internal ID6635357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4075653..4089624hg38UCSC Ensembl
Innerchr3:4075653..4089624hg38UCSC Ensembl
Outerchr3:4075153..4090124hg38UCSC Ensembl
chr3:4117337..4131308hg19UCSC Ensembl
Innerchr3:4117337..4131308hg19UCSC Ensembl
Outerchr3:4116837..4131808hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3813972
hg1913972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10903569, essv10903562, essv10903567, essv10903571, essv10903566, essv10903561, essv10903570, essv10903564, essv10903573, essv10903568, essv10903563, essv10903572, essv10903565
SamplesHG01985, NA18877, HG03199, NA19385, HG02427, NA19327, NA20903, HG04054, HG02256, HG00254, NA19019, HG03433, NA20502
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595082
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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