A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829465



Internal ID6134555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75099582..75100342hg19UCSC Ensembl
Innerchr2:74953090..74953850hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1423209
SamplesNA18999
Known GenesHK2
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv829465
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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