A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515159



Internal ID15813518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91640009..91641113hg38UCSC Ensembl
Innerchr9:94402291..94403395hg19UCSC Ensembl
Innerchr9:93442112..93443216hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381105
hg191105
hg181105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2977643, nssv2977646, nssv2977645, nssv2977648, nssv2977644, nssv2977642, nssv2977647
SamplesNA06993, NA12275, NA12760, NA12752, NA10836, NA06989, NA12329
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515159
Frequency
Sample Size2366
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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