A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595235



Internal ID6982553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9318163..9327442hg38UCSC Ensembl
Innerchr3:9318164..9327442hg38UCSC Ensembl
Outerchr3:9318163..9327443hg38UCSC Ensembl
chr3:9359847..9369126hg19UCSC Ensembl
Innerchr3:9359848..9369126hg19UCSC Ensembl
Outerchr3:9359847..9369127hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg389280
hg199280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10917560, essv10917559, essv10917565, essv10917566, essv10917568, essv10917563, essv10917561, essv10917564, essv10917567, essv10917562, essv10917558
SamplesNA20514, HG00379, HG00335, HG00325, HG00309, HG00365, HG00313, HG00176, NA20760, HG00382, NA12006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595235
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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