A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616019



Internal ID16056742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137223996..137324526hg38UCSC Ensembl
Innerchr9:140118448..140218978hg19UCSC Ensembl
Innerchr9:139238269..139338799hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38100531
hg19100531
hg18100531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13011n54
Supporting Variantsnssv1148374
Samples
Known GenesC9orf169, C9orf173, EXD3, FAM166A, LOC100129722, NELFB, NRARP, RNF224, SLC34A3, TOR4A, TUBB4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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