A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19263



Internal ID15827763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58059798..58060824hg38UCSC Ensembl
Outerchr10:58059695..58064403hg38UCSC Ensembl
Innerchr10:59819558..59820584hg19UCSC Ensembl
Outerchr10:59819455..59824163hg19UCSC Ensembl
Innerchr10:59489564..59490590hg18UCSC Ensembl
Outerchr10:59489461..59494169hg18UCSC Ensembl
Innerchr10:59489564..59490590hg17UCSC Ensembl
Outerchr10:59489461..59494169hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384709
hg194709
hg184709
hg174709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8678
Supporting Variants
SamplesNA07048
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)nssv19263
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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