A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26638



Internal ID15841954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:90096971..90125223hg38UCSC Ensembl
Outerchr16:90095961..90125699hg38UCSC Ensembl
Innerchr16:90163379..90191631hg19UCSC Ensembl
Outerchr16:90162369..90192107hg19UCSC Ensembl
Innerchr16:88690880..88719132hg18UCSC Ensembl
Outerchr16:88689870..88719608hg18UCSC Ensembl
Innerchr16:88690880..88719132hg17UCSC Ensembl
Outerchr16:88689870..88719608hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3829739
hg1929739
hg1829739
hg1729739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9483
Supporting Variants
SamplesNA19132
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)nssv26638
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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