A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614853



Internal ID16402262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90421122..90504226hg38UCSC Ensembl
Innerchr9:93183404..93266508hg19UCSC Ensembl
Innerchr9:92223224..92306328hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3883105
hg1983105
hg1883105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139318
Samples
Known GenesLOC340515
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614853
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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