A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760446



Internal ID10376754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45496768..45598106hg38UCSC Ensembl
Innerchr17:43574134..43675472hg19UCSC Ensembl
Innerchr17:40929917..41031255hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38101339
hg19101339
hg18101339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7024629, essv7024631, essv7024627, essv7024617, essv7024615, essv7024621, essv7024628, essv7024625, essv7024619, essv7024618, essv7024630, essv7024626, essv7024623, essv7024616, essv7024624, essv7024620
SamplesRW_0644, RW_0348, RW_0553, RW_0520, RW_0137, RW_0624, RW_0509, RW_0500, RW_0324, RW_0611, RW_0250, RW_0053, RW_0667, RW_0048, RW_0028, RW_0063
Known GenesLRRC37A4P
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)esv2760446
Frequency
Sample Size1109
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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