A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13009n54



Internal ID20146433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137173890..137327859hg38UCSC Ensembl
chr9:140068342..140222311hg19UCSC Ensembl
chr9:139188163..139342132hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38153970
hg19153970
hg18153970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv616015, nsv616017, nsv616016, nsv616009
Samples
Known GenesANAPC2, C9orf169, C9orf173, EXD3, FAM166A, LOC100129722, NDOR1, NELFB, NRARP, RNF208, RNF224, SLC34A3, SSNA1, TMEM203, TOR4A, TPRN, TUBB4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13009n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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