A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19675



Internal ID15840583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125886822..125905606hg38UCSC Ensembl
Outerchr10:125884747..125913319hg38UCSC Ensembl
Innerchr10:127575391..127594175hg19UCSC Ensembl
Outerchr10:127573316..127601888hg19UCSC Ensembl
Innerchr10:127565381..127584165hg18UCSC Ensembl
Outerchr10:127563306..127591878hg18UCSC Ensembl
Innerchr10:127565381..127584165hg17UCSC Ensembl
Outerchr10:127563306..127591878hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3828573
hg1928573
hg1828573
hg1728573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8738
Supporting Variants
SamplesNA18980
Known GenesFANK1
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)nssv19675
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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