A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148370



Internal ID15654870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137200153..137306303hg38UCSC Ensembl
Innerchr9:140094605..140200755hg19UCSC Ensembl
Innerchr9:139214426..139320576hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38106151
hg19106151
hg18106151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616015
Supporting Variants
Samples
Known GenesC9orf169, C9orf173, FAM166A, LOC100129722, NDOR1, NELFB, NRARP, RNF208, RNF224, SLC34A3, TMEM203, TOR4A, TPRN, TUBB4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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