A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053706



Internal ID19142925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112266396..112317519hg38UCSC Ensembl
Innerchr9:115028676..115079799hg19UCSC Ensembl
Innerchr9:114068497..114119620hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851124
hg1951124
hg1851124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759804
Samples
Known GenesMIR3134, PTBP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053706
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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