A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595733



Internal ID6983051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30226089..30304939hg38UCSC Ensembl
Innerchr3:30226092..30304937hg38UCSC Ensembl
Outerchr3:30226087..30304942hg38UCSC Ensembl
chr3:30267580..30346430hg19UCSC Ensembl
Innerchr3:30267583..30346428hg19UCSC Ensembl
Outerchr3:30267578..30346433hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3878851
hg1978851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv882e214
Supporting Variantsessv10968960, essv10968961
SamplesHG00956, HG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595733
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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