A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035363



Internal ID19124582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113119308..113147256hg38UCSC Ensembl
Innerchr9:115881588..115909536hg19UCSC Ensembl
Innerchr9:114921409..114949357hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3827949
hg1927949
hg1827949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7705n100
Supporting Variantsnssv3759811
Samples
Known GenesFAM225A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035363
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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