A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620428



Internal ID7007299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38491247..38510953hg38UCSC Ensembl
Innerchr9:38491247..38510953hg38UCSC Ensembl
Outerchr9:38490747..38511453hg38UCSC Ensembl
chr9:38491244..38510950hg19UCSC Ensembl
Innerchr9:38491244..38510950hg19UCSC Ensembl
Outerchr9:38490744..38511450hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3819707
hg1919707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13464668, essv13464669
SamplesNA19171, NA12872
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620428
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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