A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621347



Internal ID7008216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104953824..105004109hg38UCSC Ensembl
Innerchr9:104953863..105004071hg38UCSC Ensembl
Outerchr9:104953786..105004148hg38UCSC Ensembl
chr9:107716105..107766390hg19UCSC Ensembl
Innerchr9:107716144..107766352hg19UCSC Ensembl
Outerchr9:107716067..107766429hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3850286
hg1950286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13592539
SamplesHG01506
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621347
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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