A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24673



Internal ID15844009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122582945..122621018hg38UCSC Ensembl
Outerchr10:122580742..122622194hg38UCSC Ensembl
Innerchr10:124342461..124380534hg19UCSC Ensembl
Outerchr10:124340258..124381710hg19UCSC Ensembl
Innerchr10:124332451..124370524hg18UCSC Ensembl
Outerchr10:124330248..124371700hg18UCSC Ensembl
Innerchr10:124332451..124370524hg17UCSC Ensembl
Outerchr10:124330248..124371700hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3841453
hg1941453
hg1841453
hg1741453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8731
Supporting Variants
SamplesNA19221
Known GenesDMBT1
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)nssv24673
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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