A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621140



Internal ID6661320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94880452..94886100hg38UCSC Ensembl
Innerchr9:94880491..94886061hg38UCSC Ensembl
Outerchr9:94880413..94886139hg38UCSC Ensembl
chr9:97642734..97648382hg19UCSC Ensembl
Innerchr9:97642773..97648343hg19UCSC Ensembl
Outerchr9:97642695..97648421hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385649
hg195649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571504, essv13571501, essv13571503, essv13571502
SamplesHG02429, HG02558, HG02479, NA20289
Known GenesC9orf3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621140
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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