A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049453



Internal ID18791984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106461484..106604650hg38UCSC Ensembl
Innerchr9:109223765..109366931hg19UCSC Ensembl
Innerchr9:108263586..108406752hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38143167
hg19143167
hg18143167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759802
Samples
Known GenesMIR8081
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049453
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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