A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018416



Internal ID19107633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14846755..14921249hg38UCSC Ensembl
Innerchr9:14846753..14921247hg19UCSC Ensembl
Innerchr9:14836753..14911247hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3874495
hg1974495
hg1874495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690620
Samples
Known GenesFREM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018416
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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