A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv828572



Internal ID6133662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48902292..49000866hg19UCSC Ensembl
Innerchr19:53594104..53692678hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1435562
SamplesNA18942
Known GenesCYTH2, GRIN2D, GRWD1, KCNJ14, LMTK3
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv828572
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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