A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26483



Internal ID15839711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74329523..74428861hg38UCSC Ensembl
Outerchr16:74328419..74429098hg38UCSC Ensembl
Innerchr16:74363421..74462759hg19UCSC Ensembl
Outerchr16:74362317..74462996hg19UCSC Ensembl
Innerchr16:72920922..73020260hg18UCSC Ensembl
Outerchr16:72919818..73020497hg18UCSC Ensembl
Innerchr16:72920922..73020260hg17UCSC Ensembl
Outerchr16:72919818..73020497hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38100680
hg19100680
hg18100680
hg17100680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA18972
Known GenesCLEC18B, LOC283922
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)nssv26483
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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