A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614893



Internal ID16402302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93708353..93721192hg38UCSC Ensembl
Innerchr9:96470635..96483474hg19UCSC Ensembl
Innerchr9:95510456..95523295hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3812840
hg1912840
hg1812840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12797n54
Supporting Variantsnssv1139533
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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