A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26892



Internal ID15490327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:834069..914347hg38UCSC Ensembl
Outerchr1:833737..915486hg38UCSC Ensembl
Innerchr1:769449..849727hg19UCSC Ensembl
Outerchr1:769117..850866hg19UCSC Ensembl
Innerchr1:759312..839590hg18UCSC Ensembl
Outerchr1:758980..840729hg18UCSC Ensembl
Innerchr1:809312..889590hg17UCSC Ensembl
Outerchr1:808980..890729hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3881750
hg1981750
hg1881750
hg1781750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10161
Supporting Variants
SamplesNA18572
Known GenesFAM41C, LINC01128
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)nssv26892
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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