A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569366



Internal ID16010089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49252995..49254377hg38UCSC Ensembl
Innerchr15:49545192..49546574hg19UCSC Ensembl
Innerchr15:47332484..47333866hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381383
hg191383
hg181383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4518n54
Supporting Variantsnssv842838, nssv842840, nssv842836, nssv842837, nssv842839
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569366
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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