A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21709



Internal ID15490426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60376309..60376853hg38UCSC Ensembl
Outerchr17:60255220..60396836hg38UCSC Ensembl
Innerchr17:58453670..58454214hg19UCSC Ensembl
Outerchr17:58332581..58474197hg19UCSC Ensembl
Innerchr17:55808452..55808996hg18UCSC Ensembl
Outerchr17:55687363..55828979hg18UCSC Ensembl
Innerchr17:55808452..55808996hg17UCSC Ensembl
Outerchr17:55687363..55828979hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38141617
hg19141617
hg18141617
hg17141617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9581
Supporting Variants
SamplesNA18572
Known GenesUSP32
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)nssv21709
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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