A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620617



Internal ID7007487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71921613..71924873hg38UCSC Ensembl
Innerchr9:71921613..71924873hg38UCSC Ensembl
Outerchr9:71921411..71925081hg38UCSC Ensembl
chr9:74536529..74539789hg19UCSC Ensembl
Innerchr9:74536529..74539789hg19UCSC Ensembl
Outerchr9:74536327..74539997hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383261
hg193261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13514282, essv13514281, essv13514283
SamplesNA20853, NA20899, NA20892
Known GenesC9orf85
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620617
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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