A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046217



Internal ID18788748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113092059..113119308hg38UCSC Ensembl
Innerchr9:115854339..115881588hg19UCSC Ensembl
Innerchr9:114894160..114921409hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3827250
hg1927250
hg1827250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7704n100
Supporting Variantsnssv3695145
Samples
Known GenesFAM225A, FAM225B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046217
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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