A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26899



Internal ID15494358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12835552..12932211hg38UCSC Ensembl
Outerchr1:12834462..12932682hg38UCSC Ensembl
Innerchr1:12895403..12992041hg19UCSC Ensembl
Outerchr1:12894313..12992512hg19UCSC Ensembl
Innerchr1:12817990..12914628hg18UCSC Ensembl
Outerchr1:12816900..12915099hg18UCSC Ensembl
Innerchr1:12829669..12926307hg17UCSC Ensembl
Outerchr1:12828579..12926778hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3898221
hg1998200
hg1898200
hg1798200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8768
Supporting Variants
SamplesNA19007
Known GenesHNRNPCL1, LOC649330, PRAMEF10, PRAMEF2, PRAMEF4, PRAMEF7, PRAMEF8
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)nssv26899
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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