A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16391



Internal ID15485601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83855454..83978093hg38UCSC Ensembl
Outerchr9:83854808..83978843hg38UCSC Ensembl
Innerchr9:86470369..86593008hg19UCSC Ensembl
Outerchr9:86469723..86593758hg19UCSC Ensembl
Innerchr9:85660189..85782828hg18UCSC Ensembl
Outerchr9:85659543..85783578hg18UCSC Ensembl
Innerchr9:83699923..83822562hg17UCSC Ensembl
Outerchr9:83699277..83823312hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38124036
hg19124036
hg18124036
hg17124036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8541
Supporting Variants
SamplesNA12872
Known GenesC9orf64, HNRNPK, KIF27, MIR7-1
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)nssv16391
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer