A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21154



Internal ID15828578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64947869..64956441hg38UCSC Ensembl
Outerchr13:64947044..64957255hg38UCSC Ensembl
Innerchr13:65522001..65530573hg19UCSC Ensembl
Outerchr13:65521176..65531387hg19UCSC Ensembl
Innerchr13:64420002..64428574hg18UCSC Ensembl
Outerchr13:64419177..64429388hg18UCSC Ensembl
Innerchr13:64420002..64428574hg17UCSC Ensembl
Outerchr13:64419177..64429388hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3810212
hg1910212
hg1810212
hg1710212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9082
Supporting Variants
SamplesNA10839
Known Genes
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)nssv21154
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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