A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv827383



Internal ID6140423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72100044..72107239hg19UCSC Ensembl
Innerchr15:69887098..69894293hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1432438
SamplesAK20
Known GenesNR2E3
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv827383
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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