A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613637



Internal ID16054360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14524440..15011917hg38UCSC Ensembl
Innerchr9:14524438..15011915hg19UCSC Ensembl
Innerchr9:14514438..15001915hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38487478
hg19487478
hg18487478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128781
Samples
Known GenesCER1, FREM1, LOC389705, ZDHHC21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613637
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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