A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621195



Internal ID7008064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97911070..97911779hg38UCSC Ensembl
Innerchr9:97911081..97911769hg38UCSC Ensembl
Outerchr9:97911060..97911790hg38UCSC Ensembl
chr9:100673352..100674061hg19UCSC Ensembl
Innerchr9:100673363..100674051hg19UCSC Ensembl
Outerchr9:100673342..100674072hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13573740
SamplesHG02805
Known GenesC9orf156
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621195
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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