A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611839



Internal ID16399248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105784390..105785047hg38UCSC Ensembl
Innerchr8:106796618..106797275hg19UCSC Ensembl
Innerchr8:106865794..106866451hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38658
hg19658
hg18658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12252n54
Supporting Variantsnssv1118233, nssv1118234
Samples
Known GenesZFPM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611839
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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