A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv823361



Internal ID6136401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179213324..179251243hg19UCSC Ensembl
Innerchr5:179145930..179183849hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1432066
SamplesAK20
Known GenesLTC4S, MGAT4B, MIR1229, SQSTM1
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv823361
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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