A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13007n54



Internal ID19005183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136966179..137173890hg38UCSC Ensembl
chr9:139860631..140068342hg19UCSC Ensembl
chr9:138980452..139188163hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38207712
hg19207712
hg18207712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615989, nsv615990
Samples
Known GenesABCA2, C9orf139, C9orf142, CLIC3, DPP7, ENTPD2, FUT7, GRIN1, LCNL1, LRRC26, MAN1B1, MAN1B1-AS1, MIR3621, NPDC1, PTGDS, SAPCD2, TMEM210, UAP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13007n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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