A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19397



Internal ID15489098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49865290..49870782hg38UCSC Ensembl
Outerchr10:49864994..49871244hg38UCSC Ensembl
Innerchr10:51073336..51078828hg19UCSC Ensembl
Outerchr10:51073040..51079290hg19UCSC Ensembl
Innerchr10:50743342..50748834hg18UCSC Ensembl
Outerchr10:50743046..50749296hg18UCSC Ensembl
Innerchr10:50743342..50748834hg17UCSC Ensembl
Outerchr10:50743046..50749296hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg386251
hg196251
hg186251
hg176251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8640
Supporting Variants
SamplesNA18563
Known GenesPARG
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)nssv19397
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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