A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv828069



Internal ID6133159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57183476..57184487hg19UCSC Ensembl
Innerchr17:54538258..54539269hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1432516
SamplesAK20
Known GenesTRIM37
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv828069
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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