A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594884



Internal ID6635159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134250..171681hg38UCSC Ensembl
Innerchr3:134250..171681hg38UCSC Ensembl
Outerchr3:133750..172181hg38UCSC Ensembl
chr3:175933..213364hg19UCSC Ensembl
Innerchr3:175933..213364hg19UCSC Ensembl
Outerchr3:175433..213864hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3837432
hg1937432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10896260, essv10896261
SamplesHG01880, HG02238
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594884
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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