A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21327



Internal ID15841675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62013294..62036048hg38UCSC Ensembl
Outerchr9:62012700..62036351hg38UCSC Ensembl
Innerchr9:67620107..67642865hg19UCSC Ensembl
Outerchr9:67619804..67643459hg19UCSC Ensembl
Innerchr9:67209927..67232685hg18UCSC Ensembl
Outerchr9:67209624..67233279hg18UCSC Ensembl
Innerchr9:66110272..66133030hg17UCSC Ensembl
Outerchr9:66109969..66133624hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3823652
hg1923656
hg1823656
hg1723656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8499
Supporting Variants
SamplesNA19132
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv21327
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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