A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13010n54



Internal ID22780905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137191539..137233413hg38UCSC Ensembl
chr9:140085991..140127865hg19UCSC Ensembl
chr9:139205812..139247686hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3841875
hg1941875
hg1841875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv616011, nsv616014, nsv616013
Samples
Known GenesC9orf169, NDOR1, RNF208, RNF224, SLC34A3, TMEM203, TPRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13010n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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