A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615842



Internal ID16403251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135113632..135571320hg38UCSC Ensembl
Innerchr9:138005478..138463166hg19UCSC Ensembl
Innerchr9:137145299..137602987hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38457689
hg19457689
hg18457689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1146786
Samples
Known GenesC9orf116, C9orf62, LCN1, LOC401557, MRPS2, OBP2A, OLFM1, PAEP, PPP1R26, PPP1R26-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615842
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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