A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566



Internal ID15488574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38545026..38571021hg38UCSC Ensembl
Outerchr9:38544049..38572042hg38UCSC Ensembl
Innerchr9:38545023..38571018hg19UCSC Ensembl
Outerchr9:38544046..38572039hg19UCSC Ensembl
Innerchr9:38535023..38561018hg18UCSC Ensembl
Outerchr9:38534046..38562039hg18UCSC Ensembl
Innerchr9:38535023..38561018hg17UCSC Ensembl
Outerchr9:38534046..38562039hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3827994
hg1927994
hg1827994
hg1727994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8445
Supporting Variants
SamplesNA18552
Known GenesANKRD18A, FAM95C
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)nssv17566
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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