A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7014186



Internal ID10338795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103290101..103314186hg38UCSC Ensembl
Innerchr6:103737976..103762061hg19UCSC Ensembl
Innerchr6:103844669..103868754hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3824086
hg1924086
hg1824086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761041
Supporting Variants
SamplesRW_0187
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)essv7014186
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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