A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7006661



Internal ID9985659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169599408..169603107hg38UCSC Ensembl
Innerchr1:169568646..169572345hg19UCSC Ensembl
Innerchr1:167835270..167838969hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg383700
hg193700
hg183700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2762197
Supporting Variants
SamplesRW_0020
Known GenesSELP
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)essv7006661
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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