A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2761558



Internal ID10028911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124729643..124808848hg38UCSC Ensembl
Innerchr9:127491922..127571127hg19UCSC Ensembl
Innerchr9:126531743..126610948hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3879206
hg1979206
hg1879206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6994368
SamplesSW_0690
Known GenesNR6A1, OLFML2A
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)esv2761558
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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