A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620165



Internal ID7007038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28507832..28644880hg38UCSC Ensembl
Innerchr9:28508332..28644380hg38UCSC Ensembl
Outerchr9:28506832..28645880hg38UCSC Ensembl
chr9:28507830..28644878hg19UCSC Ensembl
Innerchr9:28508330..28644378hg19UCSC Ensembl
Outerchr9:28506830..28645878hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38137049
hg19137049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13436653, essv13436652
SamplesHG04195, HG04017
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620165
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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