A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598811



Internal ID6972329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178035773..178039411hg38UCSC Ensembl
Innerchr3:178035792..178039393hg38UCSC Ensembl
Outerchr3:178035755..178039430hg38UCSC Ensembl
chr3:177753561..177757199hg19UCSC Ensembl
Innerchr3:177753580..177757181hg19UCSC Ensembl
Outerchr3:177753543..177757218hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383639
hg193639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11238488, essv11238490, essv11238483, essv11238481, essv11238489, essv11238487, essv11238484, essv11238482, essv11238485, essv11238486
SamplesHG02614, NA18508, HG02621, HG02756, HG02860, HG03380, HG03391, HG01403, NA19035, HG02282
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598811
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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