A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv823889



Internal ID6136929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158614538..158682796hg19UCSC Ensembl
Innerchr6:158534526..158602784hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1435148
SamplesNA18942
Known GenesGTF2H5
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv823889
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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