A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619630



Internal ID7006504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11732199..12016115hg38UCSC Ensembl
Innerchr9:11732699..12015615hg38UCSC Ensembl
Outerchr9:11731199..12017115hg38UCSC Ensembl
chr9:11732199..12016115hg19UCSC Ensembl
Innerchr9:11732699..12015615hg19UCSC Ensembl
Outerchr9:11731199..12017115hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38283917
hg19283917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1445e214
Supporting Variantsessv13403628, essv13403632, essv13403631, essv13403627, essv13403626, essv13403630, essv13403629
SamplesHG03773, HG01506, NA18747, NA18939, NA18610, HG00123, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619630
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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