A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22613



Internal ID15839556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125884107..125899708hg38UCSC Ensembl
Outerchr10:125883224..125900500hg38UCSC Ensembl
Innerchr10:127572676..127588277hg19UCSC Ensembl
Outerchr10:127571793..127589069hg19UCSC Ensembl
Innerchr10:127562666..127578267hg18UCSC Ensembl
Outerchr10:127561783..127579059hg18UCSC Ensembl
Innerchr10:127562666..127578267hg17UCSC Ensembl
Outerchr10:127561783..127579059hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817277
hg1917277
hg1817277
hg1717277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8738
Supporting Variants
SamplesNA18972
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)nssv22613
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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