A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620577



Internal ID7007447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70366039..70369245hg38UCSC Ensembl
Innerchr9:70366065..70369220hg38UCSC Ensembl
Outerchr9:70366014..70369271hg38UCSC Ensembl
chr9:72980955..72984161hg19UCSC Ensembl
Innerchr9:72980981..72984136hg19UCSC Ensembl
Outerchr9:72980930..72984187hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg383207
hg193207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13512321
SamplesHG01852
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620577
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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