A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv828452



Internal ID6133542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14170554..14258966hg19UCSC Ensembl
Innerchr19:14031554..14119966hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1435549
SamplesNA18942
Known GenesASF1B, LOC113230, LPHN1, PRKACA, SAMD1
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv828452
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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