A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6993668



Internal ID10011267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21642610..21657075hg38UCSC Ensembl
Innerchr9:21642609..21657074hg19UCSC Ensembl
Innerchr9:21632609..21647074hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3814466
hg1914466
hg1814466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2764150
Supporting Variants
SamplesSW_0632
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)essv6993668
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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