A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13012n54



Internal ID20146436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137478118..137641646hg38UCSC Ensembl
chr9:140372570..140536098hg19UCSC Ensembl
chr9:139492391..139655919hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38163529
hg19163529
hg18163529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv616024, nsv616022
Samples
Known GenesARRDC1, C9orf37, DPH7, EHMT1, MRPL41, PNPLA7, ZMYND19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13012n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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