A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990833



Internal ID10353414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62526795..62663696hg38UCSC Ensembl
Innerchr7:61987173..62124074hg19UCSC Ensembl
Innerchr7:61624608..61761509hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38136902
hg19136902
hg18136902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2764031
Supporting Variants
SamplesSW_0103
Known Genes
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)essv6990833
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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