A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21174



Internal ID15840188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21001063..21008219hg38UCSC Ensembl
Outerchr15:20999794..21011273hg38UCSC Ensembl
Innerchr15:21206392..21213548hg19UCSC Ensembl
Outerchr15:21205123..21216602hg19UCSC Ensembl
Innerchr15:19471051..19478207hg18UCSC Ensembl
Outerchr15:19469782..19481261hg18UCSC Ensembl
Innerchr15:19471051..19478207hg17UCSC Ensembl
Outerchr15:19469782..19481261hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811480
hg1911480
hg1811480
hg1711480
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18975
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)nssv21174
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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