A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619631



Internal ID7006505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11750067..12080970hg38UCSC Ensembl
Innerchr9:11750567..12080470hg38UCSC Ensembl
Outerchr9:11749067..12081970hg38UCSC Ensembl
chr9:11750067..12080970hg19UCSC Ensembl
Innerchr9:11750567..12080470hg19UCSC Ensembl
Outerchr9:11749067..12081970hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38330904
hg19330904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1445e214
Supporting Variantsessv13403639, essv13403633, essv13403637, essv13403638, essv13403635, essv13403636, essv13403634
SamplesHG03773, NA19222, NA18939, NA21141, HG01812, NA18610, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619631
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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