A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7025713



Internal ID9998427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42816985..42992589hg38UCSC Ensembl
Innerchr19:43321137..43496741hg19UCSC Ensembl
Innerchr19:48012977..48188581hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38175605
hg19175605
hg18175605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760524
Supporting Variants
SamplesRW_0502
Known GenesLOC100289650, PSG1, PSG10P, PSG6, PSG7
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)essv7025713
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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