A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7031953



Internal ID10008888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29055437..29181665hg38UCSC Ensembl
Innerchr6:29023214..29149442hg19UCSC Ensembl
Innerchr6:29131193..29257421hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38126229
hg19126229
hg18126229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763545
Supporting Variants
SamplesSW_0255
Known GenesLOC100129636, OR2B3, OR2J2, OR2J3
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)essv7031953
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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