A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15701



Internal ID15832027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33603872..33608906hg38UCSC Ensembl
Outerchr9:33598658..33611084hg38UCSC Ensembl
Innerchr9:33603870..33608904hg19UCSC Ensembl
Outerchr9:33598656..33611082hg19UCSC Ensembl
Innerchr9:33593870..33598904hg18UCSC Ensembl
Outerchr9:33588656..33601082hg18UCSC Ensembl
Innerchr9:33593870..33598904hg17UCSC Ensembl
Outerchr9:33588656..33601082hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3812427
hg1912427
hg1812427
hg1712427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8440
Supporting Variants
SamplesNA12872
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)nssv15701
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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