A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555



Internal ID15829046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50707853..50709420hg38UCSC Ensembl
Outerchr10:50706589..50709574hg38UCSC Ensembl
Innerchr10:52467613..52469180hg19UCSC Ensembl
Outerchr10:52466349..52469334hg19UCSC Ensembl
Innerchr10:52137619..52139186hg18UCSC Ensembl
Outerchr10:52136355..52139340hg18UCSC Ensembl
Innerchr10:52137619..52139186hg17UCSC Ensembl
Outerchr10:52136355..52139340hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382986
hg192986
hg182986
hg172986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8663
Supporting Variants
SamplesNA10847
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)nssv17555
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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