A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7031897



Internal ID10012333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10467462..10530771hg38UCSC Ensembl
Innerchr6:10467695..10531004hg19UCSC Ensembl
Innerchr6:10575681..10638990hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3863310
hg1963310
hg1863310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763942
Supporting Variants
SamplesSW_0703
Known GenesGCNT2
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)essv7031897
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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