A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576



Internal ID15840982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81708923..81709419hg38UCSC Ensembl
Outerchr9:81708348..81712130hg38UCSC Ensembl
Innerchr9:84323838..84324334hg19UCSC Ensembl
Outerchr9:84323263..84327045hg19UCSC Ensembl
Innerchr9:83513658..83514154hg18UCSC Ensembl
Outerchr9:83513083..83516865hg18UCSC Ensembl
Innerchr9:81553392..81553888hg17UCSC Ensembl
Outerchr9:81552817..81556599hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg383783
hg193783
hg183783
hg173783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8533
Supporting Variants
SamplesNA19007
Known GenesLOC101927502
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)nssv17576
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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